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

AXIOM VESSEL LOOPS

K Number: K800015 · Decision Mar 25, 1980
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
28
Review Days
81

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Basic Information

Device Name
AXIOM VESSEL LOOPS
K Number
K800015
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Axiom Medical, Inc.
Date Received
January 4, 1980
Decision Date
March 25, 1980
Product Code
KDC
Advisory Committee
General, Plastic Surgery
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
KDC Instrument, Surgical, Disposable

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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
K922760 ATRAUM WOUND DRESSING--MODIFICATION
K905422 PVC ROUND WOUND DRAINS
K904218 SUCTION SYSTEM
K904133 DISPOSABLE FLUID COLLECTION BAG
K863247 AXIOM TROCAR THORACIC CATHETER
K861306 SUCTION SYSTEM
Search all 28 clearances from Axiom Medical, Inc. →