CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL— 510(k) K021676

Name: FDA 510(k) clearance K021676
Creator: U.S. Food and Drug Administration
Published: 2002-07-12

Substantially Equivalent

Cypress Medical Products, Ltd.

FDA 510(k) clearance K021676 for CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL, Substantially Equivalent on 2002-07-12. Applicant: Cypress Medical Products, Ltd.. Device class: 2.

Clearance details

Applicant: Cypress Medical Products, Ltd.
Product code: Code HIB
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 2002-05-21
Decision date: 2002-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mc Henry, IL, US

Download summary PDF View on FDA.gov ↗

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