FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ATRAUM WOUND DRESSING--MODIFICATION

K Number: K922760 · Decision Oct 30, 1992
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
28
Review Days
155

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Basic Information

Device Name
ATRAUM WOUND DRESSING--MODIFICATION
K Number
K922760
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Axiom Medical, Inc.
Date Received
May 28, 1992
Decision Date
October 30, 1992
Product Code
KMF
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KMF Bandage, Liquid

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Other Clearances by Axiom Medical, Inc.

K Number Device Name
K993592 AXIOM MULTIPURPOSE WOUND DRAIN
K971851 INTERPLEURAL ANESTHESIA CATHETER
K965146 FLAT CLOSED WOUND DRAIN WITH TROCAR
K934895 GLASSMAN SILICONE CATHETER
K905422 PVC ROUND WOUND DRAINS
K904218 SUCTION SYSTEM
K904133 DISPOSABLE FLUID COLLECTION BAG
K863247 AXIOM TROCAR THORACIC CATHETER
K861306 SUCTION SYSTEM
K852614 ATRAUM WOUND DRESSING
Search all 28 clearances from Axiom Medical, Inc. →