PREP-SITE PROTECTIVE DRESSING WIPE— 510(k) K811625

Name: FDA 510(k) clearance K811625
Creator: U.S. Food and Drug Administration
Published: 1981-07-10

Substantially Equivalent

Acme United Corp.

FDA 510(k) clearance K811625 for PREP-SITE PROTECTIVE DRESSING WIPE, Substantially Equivalent on 1981-07-10. Applicant: Acme United Corp.. Device class: 1.

Clearance details

Applicant: Acme United Corp.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1981-06-09
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMF

view all

K241916 — TearRepair Liquid Skin Protectant2024-09-27
K182733 — Rochal Bioshield Silicone Film2019-06-27
K171148 — Aleo BME Liquid Bandage2018-01-12
K153571 — Cavilon Advanced High Endurance Skin Protectant2016-08-23
K160684 — Atteris No-Sting Skin Protectant2016-07-26

More clearances from Acme United Corp.

view all

K961323 — LYOFOAM EXTRA C ODOR ABSORBING WOUND DRESSING1996-06-19
K961452 — LYOFOAM EXTRA 'A' STERILE ADHESIVE WOUND DRESSING1996-05-31
K952565 — LYOFOAM EXTRA1995-11-14
K895764 — MODIFIED LYOFOAM WOUND DRESSINGS1990-09-10
K871740 — LYOSHEET SURGICAL SHEET FOR BURNS1987-06-09

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