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

POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE

K Number: K872182 · Decision Oct 30, 1987
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
8
Review Days
144

Basic Information

Device Name
POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE
K Number
K872182
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
POLYSTAN C/O VITALCOR, INC.
Date Received
June 8, 1987
Decision Date
October 30, 1987
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

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K874853 POLYSTAN TWO STAGE CATHETERS
K874852 POLYSTAN WIRE REINFORCED TWO STAGE CATHETERS
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