MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM— 510(k) K863274

Name: FDA 510(k) clearance K863274
Creator: U.S. Food and Drug Administration
Published: 1986-09-02

Substantially Equivalent

Martin Medical

FDA 510(k) clearance K863274 for MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM, Substantially Equivalent on 1986-09-02. Applicant: Martin Medical. Device class: 2.

Clearance details

Applicant: Martin Medical
Product code: Code HIB
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1986-08-25
Decision date: 1986-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Desoto, KS, US

Download summary PDF View on FDA.gov ↗

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