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

POLYSTAN TWO STAGE CATHETERS

K Number: K874853 · Decision Feb 5, 1988
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
8
Review Days
72

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Basic Information

Device Name
POLYSTAN TWO STAGE CATHETERS
K Number
K874853
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Polystan C/O Vitalcor, Inc.
Date Received
November 25, 1987
Decision Date
February 5, 1988
Product Code
DWF
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
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Similar 510(k) Clearances

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

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Other Clearances by Polystan C/O Vitalcor, Inc.

K Number Device Name
K894657 POLYSTAN HEART-LUNG MACHINE SYSTEM
K893940 POLYSTAN HEATER-COOLER UNIT
K893705 SAFE-1 VENOUS RESERVOIR
K893704 SAFE-1
K874852 POLYSTAN WIRE REINFORCED TWO STAGE CATHETERS
K872182 POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE
K843538 PO 2 LYTRODE