KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING— 510(k) K973509

Name: FDA 510(k) clearance K973509
Creator: U.S. Food and Drug Administration
Published: 1997-12-04

Substantially Equivalent for Some Indications

Kendall Healthcare Products Co. Div.Of Tyco Health

FDA 510(k) clearance K973509 for KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING, Substantially Equivalent for Some Indications on 1997-12-04. Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health. Device class: 1.

Clearance details

Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1997-09-16
Decision date: 1997-12-04
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Mansfield, MA, US

Download summary PDF View on FDA.gov ↗

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K973507 — KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)1997-12-15
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Data sourced from openFDA. This site is unofficial and independent of the FDA.