O.R. TOWELS (STERILE)— 510(k) K890709

Name: FDA 510(k) clearance K890709
Creator: U.S. Food and Drug Administration
Published: 1989-03-14

Substantially Equivalent

Cypress Medical Products, Ltd.

FDA 510(k) clearance K890709 for O.R. TOWELS (STERILE), Substantially Equivalent on 1989-03-14. Applicant: Cypress Medical Products, Ltd.. Device class: 2.

Clearance details

Applicant: Cypress Medical Products, Ltd.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1989-02-13
Decision date: 1989-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mc Henry, IL, US

Download summary PDF View on FDA.gov ↗

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