The following data is part of a premarket notification filed by Microtest with the FDA for Microtest Multi Microbe Medium.
Device ID | K910526 |
510k Number | K910526 |
Device Name: | MICROTEST MULTI MICROBE MEDIUM |
Classification | Culture Media, Non-propagating Transport |
Applicant | MICROTEST 1379 BRENTFORD COVE Snelleville, GA 30278 |
Contact | Stephen G Racioppi |
Correspondent | Stephen G Racioppi MICROTEST 1379 BRENTFORD COVE Snelleville, GA 30278 |
Product Code | JSM |
CFR Regulation Number | 866.2390 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-02-07 |
Decision Date | 1991-04-09 |