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

SUCTION SYSTEM

K Number: K861306 · Decision Jun 9, 1986
Classifications
1
FEI Numbers
378
Registration Numbers
378
Same Product Code
35
Applicant Total
28
Review Days
62

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Basic Information

Device Name
SUCTION SYSTEM
K Number
K861306
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
April 8, 1986
Decision Date
June 9, 1986
Product Code
GEA
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
GEA Cannula, Surgical, General & Plastic Surgery

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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
K852614 ATRAUM WOUND DRESSING
Search all 28 clearances from Axiom Medical, Inc. →