PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY— 510(k) K955790

Name: FDA 510(k) clearance K955790
Creator: U.S. Food and Drug Administration
Published: 1996-03-21

Substantially Equivalent

Trylon Corp.

FDA 510(k) clearance K955790 for PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY, Substantially Equivalent on 1996-03-21. Applicant: Trylon Corp.. Device class: 2.

Clearance details

Applicant: Trylon Corp.
Product code: Code HIC
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1995-12-22
Decision date: 1996-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Monarch Beach, CA, 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.