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

AXIOM ATRAUM TROCAR CATHETER

K Number: K852241 · Decision Jun 14, 1985
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
26
Applicant Total
28
Review Days
22

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Basic Information

Device Name
AXIOM ATRAUM TROCAR CATHETER
K Number
K852241
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Axiom Medical, Inc.
Date Received
May 23, 1985
Decision Date
June 14, 1985
Product Code
GBS
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
GBS Catheter, Ventricular, General & Plastic Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBS), ordered by most recent decision date.

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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. →