IMPROVED THAYER MARTIN MEDIUM

Culture Media, For Isolation Of Pathogenic Neisseria

BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC

The following data is part of a premarket notification filed by Bd Becton Dickinson Vacutainer Systems Preanalytic with the FDA for Improved Thayer Martin Medium.

Pre-market Notification Details

• Device ID: K760588
• 510k Number: K760588
• Device Name: IMPROVED THAYER MARTIN MEDIUM
• Classification: Culture Media, For Isolation Of Pathogenic Neisseria
• Applicant: BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC 1875 EYE ST. NW STE. 625 Washington, DC 20006
• Product Code: JTY
• CFR Regulation Number: 866.2410 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1976-09-03
• Decision Date: 1976-10-07

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
30382902216231	K760588	000
30382902215678	K760588	000
30382902215685	K760588	000