PC-BEADS POSTCOITAL TEST— 510(k) K902995

Name: FDA 510(k) clearance K902995
Creator: U.S. Food and Drug Administration
Published: 1991-01-31

Substantially Equivalent

Microscopy Research Innovations

FDA 510(k) clearance K902995 for PC-BEADS POSTCOITAL TEST, Substantially Equivalent on 1991-01-31. Applicant: Microscopy Research Innovations. Device class: 2.

Clearance details

Applicant: Microscopy Research Innovations
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1990-07-09
Decision date: 1991-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Knoxville, TN, US

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