FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AXIOM FEMORAL VENUS CATHETER

K Number: K842084 · Decision Aug 1, 1984
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
28
Review Days
69

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Basic Information

Device Name
AXIOM FEMORAL VENUS CATHETER
K Number
K842084
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Axiom Medical, Inc.
Date Received
May 24, 1984
Decision Date
August 1, 1984
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQY Catheter, Percutaneous

Similar 510(k) Clearances

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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. →