PF TEST— 510(k) K884513

Substantially Equivalent

Medi-Tech, Inc.

FDA 510(k) clearance K884513 for PF TEST, Substantially Equivalent on 1989-02-03. Applicant: Medi-Tech, Inc.. Device class: 1.

Clearance details

Applicant: Medi-Tech, Inc.
Product code: Code GMZ
Device class: Class 1
Regulation: 21 CFR 866.3255
Advisory panel: Microbiology
Date received: 1988-10-27
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, NJ, US

Download summary PDF View on FDA.gov ↗

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