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 ID: BK920013
• 510k Number: BK920013
• Device Name: Potentiating Media For In Vitro Diagnostic Use
• Classification: Media, Potentiating For In Vitro Diagnostic Use
• Applicant: Micro Typing Systems Inc. 1295 S.w. 29th Ave. Pompano Beach, FL 33069
• Product Code: KSG
• CFR Regulation Number: 864.9600 [🔎]
• Decision: Substantially Equivalent (SE)
• Type: 510(k) Traditio
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-04-24
• Decision Date: 1993-09-29

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10758750006038	BK920013	0