REDITEST STREP A TEST KIT— 510(k) K903194
Substantially EquivalentBoehringer Mannheim Corp.
FDA 510(k) clearance K903194 for REDITEST STREP A TEST KIT, Substantially Equivalent on 1990-08-22. Applicant: Boehringer Mannheim Corp.. Device class: 1.
Clearance details
- Applicant
- Boehringer Mannheim Corp.
- Product code
- Code GTZ
- Device class
- Class 1
- Regulation
- 21 CFR 866.3740
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Indianapolis, IN, US
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More clearances from Boehringer Mannheim Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.