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

CENTRAL VEIN CATHERIZATION TRAY CC-20

K Number: K834073 · Decision Feb 28, 1984
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
13
Review Days
95

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Basic Information

Device Name
CENTRAL VEIN CATHERIZATION TRAY CC-20
K Number
K834073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Packaging Technologies, Inc.
Date Received
November 25, 1983
Decision Date
February 28, 1984
Product Code
FOZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Similar 510(k) Clearances

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

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Other Clearances by Packaging Technologies, Inc.

K Number Device Name
K881756 STERILE SURGEONS GLOVES
K863326 BONE MARROW TRAY
K861041 ENHANCE
K850544 SHAVE PREP TRAY
K850438 RENAL BIOPSY TRAY
K844613 GENERAL PURPOSE INSTRUMENT TRAYS SUTURE REMOVAL TR
K844611 SINGLE BASIN SET
K844614 IV START KIT
K844612 ACUTE HEMODIALYSIS TRAYS
K834074 PERCUTANEOUS SHEATH INTRODUCER TRAY
Search all 13 clearances from Packaging Technologies, Inc. →