STERILE DRAPE 17X18 W/3 FENESTRATION— 510(k) K801033

Name: FDA 510(k) clearance K801033
Creator: U.S. Food and Drug Administration
Published: 1980-05-20

Substantially Equivalent

Veratex Corp.

FDA 510(k) clearance K801033 for STERILE DRAPE 17X18 W/3 FENESTRATION, Substantially Equivalent on 1980-05-20. Applicant: Veratex Corp.. Device class: 2.

Clearance details

Applicant: Veratex Corp.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1980-05-01
Decision date: 1980-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K830175 — STERILE COTTON ROLLS #3, 1 1/21983-02-18
K801032 — STERILE DRAPE 17X18 CODE D-6A1980-05-20

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