OXOID STREPTOCOCAL GROUPING KIT— 510(k) K854929
Substantially EquivalentOxoid U.S.A., Inc.
FDA 510(k) clearance K854929 for OXOID STREPTOCOCAL GROUPING KIT, Substantially Equivalent on 1986-03-11. Applicant: Oxoid U.S.A., Inc.. Device class: 1.
Clearance details
- Applicant
- Oxoid U.S.A., Inc.
- 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
- Columbia, MD, US
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More clearances from Oxoid U.S.A., Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.