Category: FDA

FDA 21 CFR PART 806
MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Format:PDF
Language (s):English
Published:04/01/2020
FDA 21 CFR PART 807
ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Format:PDF
Language (s):English
Published:04/01/2018
FDA 21 CFR PART 807
ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
Format:PDF
Language (s):English
Published:04/01/2019
FDA 21 CFR PART 812
INVESTIGATIONAL DEVICE EXEMPTIONS
Format:PDF
Language (s):English
Published:04/01/2024
FDA 21 CFR PART 820
QUALITY SYSTEM REGULATION
Format:PDF
Language (s):English
Published:04/01/2021
FDA 21 CFR PART 820
QUALITY SYSTEM REGULATION
Format:PDF
Language (s):English
Published:04/01/2017
FDA 21 CFR PART 820
QUALITY SYSTEM REGULATION
Format:PDF
Language (s):English
Published:04/01/2019
FDA 21 CFR PART 820
QUALITY SYSTEM REGULATION
Format:PDF
Language (s):English
Published:04/01/2018
FDA 21 CFR PART 820
QUALITY SYSTEM REGULATION
Format:PDF
Language (s):English
Published:04/01/2020
FDA 21 CFR PART 821
MEDICAL DEVICE TRACKING REQUIREMENTS
Format:PDF
Language (s):English
Published:04/01/2017
FDA 21 CFR PART 830
UNIQUE DEVICE IDENTIFICATION
Format:PDF
Language (s):English
Published:04/01/2019
FDA 21 CFR PART 830
UNIQUE DEVICE IDENTIFICATION
Format:PDF
Language (s):English
Published:04/01/2018
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