STERIGAUZE WET DRESSING— 510(k) K952420

Name: FDA 510(k) clearance K952420
Creator: U.S. Food and Drug Administration
Published: 1995-07-12

Substantially Equivalent

Acacia Laboratories, Inc.

FDA 510(k) clearance K952420 for STERIGAUZE WET DRESSING, Substantially Equivalent on 1995-07-12. Applicant: Acacia Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Acacia Laboratories, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1995-05-23
Decision date: 1995-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Acacia Laboratories, Inc.

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K952419 — STERIGAUZE GEL DRESSING1995-07-26
K951861 — STERICARE WOUND CARE GEL1995-07-11
K952414 — PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER1995-06-23
K951914 — HYDRACARE ABSORBENT WOUND DRESSING1995-05-15
K950344 — HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER1995-03-24

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