CURASORB ZN ALGINATE WOUND DRESSING— 510(k) K950775

Name: FDA 510(k) clearance K950775
Creator: U.S. Food and Drug Administration
Published: 1995-04-03

Substantially Equivalent

Kendall Healthcare Products Co. Div.Of Tyco Health

FDA 510(k) clearance K950775 for CURASORB ZN ALGINATE WOUND DRESSING, Substantially Equivalent on 1995-04-03. 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: 1995-02-21
Decision date: 1995-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mansfield, MA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Kendall Healthcare Products Co. Div.Of Tyco Health

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K973763 — KENDALL CURITY IODOFORM PACKING STRIP1997-12-31
K973511 — KENDALL CURITY PETROLATUM GAUZE1997-12-16
K973507 — KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)1997-12-15
K973619 — KENDALL CURITY NON-ADHERING DRESSING1997-12-10
K973509 — KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING1997-12-04

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