PROTEUS OX-19 IFA*— 510(k) K885110

Name: FDA 510(k) clearance K885110
Creator: U.S. Food and Drug Administration
Published: 1989-08-15

Substantially Equivalent

Investigacion Farmaceutica S.A. DE C.V.

FDA 510(k) clearance K885110 for PROTEUS OX-19 IFA*, Substantially Equivalent on 1989-08-15. Applicant: Investigacion Farmaceutica S.A. DE C.V.. Device class: 1.

Clearance details

Applicant: Investigacion Farmaceutica S.A. DE C.V.
Product code: Code GSZ
Device class: Class 1
Regulation: 21 CFR 866.3410
Advisory panel: Microbiology
Date received: 1988-12-12
Decision date: 1989-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mexico, MX

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.