> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Latest Federal Register Notices
- URL: https://www.fdaweb.com/latest-federal-register-notices-14/
- Published: 2020-03-01T12:00:00.000Z
- Updated: 2026-09-14T16:05:08.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146220

[**CDRH 510(k) eSubmission Template Pilot**](https://www.fdaweb.com/cdrh-510-k-esubmission-template-pilot/)  
*Federal Register* notice: CDRH has announced a voluntary “Electronic Submission Template and Resource (eSTAR) Pilot.” 02/27/2020  

[**Standardized Medicated Feed Assay Limits Guide**](https://www.fdaweb.com/standardized-medicated-feed-assay-limits-guide/)  
*Federal Register* notice: FDA makes available a draft guidance for industry #264 entitled “Standardized Medicated Feed Assay Limits.” 02/27/2020  

[**Dual 510(k)/CLIA Waiver Guide**](https://www.fdaweb.com/dual-510-k-clia-waiver-guide/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Recommendations for Dual 510(k) and CLIA Waiver by Application Studies.” 02/26/2020  

[**Guide on Laparoscopic Power Morcellators Labeling**](https://www.fdaweb.com/guide-on-laparoscopic-power-morcellators-labeling/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “Product Labeling for Laparoscopic Power Morcellators.” 02/26/2020  

[**Guide on CLIA Waiver for IVD Devices**](https://www.fdaweb.com/guide-on-clia-waiver-for-ivd-devices/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices.” 02/26/2020  

[**Final Guide on Esubmission in eCTD Format**](https://www.fdaweb.com/final-guide-on-esubmission-in-ectd-format/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Providing Regulatory Submissions in Electronic Format — Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications (Revision 7).” 02/24/2020  

[**Comments Sought on eCTD Tech Conformance Guide**](https://www.fdaweb.com/comments-sought-on-ectd-tech-conformance-guide/)  
*Federal Register* notice: FDA seeks comments on a draft Electronic Common Technical Document v4.0 Technical Conformance Guide and the FDA eCTD v4.0 Module 1 Implementation Package. 02/24/2020  

[**Panel to Review Peanut Allergy Therapy**](https://www.fdaweb.com/panel-to-review-peanut-allergy-therapy/)  
*Federal Register* notice: FDA announces a 5/15 Allergenic Products Advisory Committee meeting to review DBV Technologies’ Peanut (Arachis hypogaea) Allergen Extract. 02/24/2020