Downloads & Documents 21 CFR 809 In Vitro Diagnostic Products for Human Use with TOC Posted on March 20, 2022April 20, 2022 by QS Compliance 21 CFR 809 In Vitro Diagnostic Products for Human Use with TOC 21 CFR 810 Medical Device Recall Authority with TOC 21 CFR 807 Establishment Registration and Device Listing with TOC
