Modified Lyofoam Wound Dressings

FDA 510(k) K895764 · Acme United Corp.

Substantially Equivalent for Some Indications

510(k) numberK895764

Submission

Device name
Modified Lyofoam Wound Dressings
Applicant
Acme United Corp.
Fairfield, CT, US
Received
September 26, 1989
Decision date
September 10, 1990
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KMF – Bandage, Liquid
Device class
Class I (low risk)
Regulation
21 CFR 880.5090
Specialty
General Hospital

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More from Polichem S.A

510(k)DeviceDecision
K961323Lyofoam Extra C Odor Absorbing Wound DressingKMF · Traditional 06/19/1996SE
K961452Lyofoam Extra 'A' Sterile Adhesive Wound DressingKMF · Traditional 05/31/1996SE
K952565Lyofoam ExtraKMF · Traditional 11/14/1995SN
K871740Lyosheet Surgical Sheet for BurnsFPY · Traditional 06/09/1987SE
K864084Lyofoam C Odor-Absorbing DressingFRO · Traditional 11/21/1986SN
K860085Lyofoam Wound DressingsNAD · Traditional 06/27/1986SN
K860818One Time Enteral Feeding BagKNT · Traditional 05/15/1986SE
K861015One Time Hyperal & Catheter Dressing Change TraysFOZ · Traditional 04/22/1986SE
K842186Acu-Derm Transparent Wound DressingNAD · Traditional 08/24/1984SE
K842064Acu-Derm Transparent IV DressingKMK · Traditional 08/15/1984SE

Questions and answers

When was Modified Lyofoam Wound Dressings cleared by the FDA?

Modified Lyofoam Wound Dressings (K895764) received a 510(k) decision of Substantially Equivalent for Some Indications on September 10, 1990, 349 days after the submission was received.

What is the product code of K895764?

The FDA product code is KMF – Bandage, Liquid, a Class I (low risk) device regulated under 21 CFR 880.5090.