STAPHYTECT PLUS/DRYSPOT STAPHYTECT PLUS— 510(k) K972030

Name: FDA 510(k) clearance K972030
Creator: U.S. Food and Drug Administration
Published: 1997-09-08

Substantially Equivalent

Oxoid , Ltd.

FDA 510(k) clearance K972030 for STAPHYTECT PLUS/DRYSPOT STAPHYTECT PLUS, Substantially Equivalent on 1997-09-08. Applicant: Oxoid , Ltd.. Device class: 1.

Clearance details

Applicant: Oxoid , Ltd.
Product code: Code JWX
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1997-06-02
Decision date: 1997-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Basingstoke, GB

Download summary PDF View on FDA.gov ↗

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