Potentiating Media For In Vitro Diagnostic Use

Media, Potentiating For In Vitro Diagnostic Use

Micro Typing Systems Inc.

The following data is part of a premarket notification filed by Micro Typing Systems Inc. with the FDA for Potentiating Media For In Vitro Diagnostic Use.

Pre-market Notification Details

Device IDBK930030
510k NumberBK930030
Device Name:Potentiating Media For In Vitro Diagnostic Use
ClassificationMedia, Potentiating For In Vitro Diagnostic Use
Applicant Micro Typing Systems Inc. 1295 S.w. 29th Ave. Pompano Beach,  FL  33069
Product CodeKSG  
CFR Regulation Number864.9600 [🔎]
DecisionSubstantially Equivalent (SE)
Type510(k) Traditio
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-10-06
Decision Date1994-01-12

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
10758750006045 BK930030 0

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.