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

TYGON TUBING

K Number: K803277 · Decision Jan 13, 1981
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
20
Applicant Total
41
Review Days
15

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Basic Information

Device Name
TYGON TUBING
K Number
K803277
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4390
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Electromedics, Inc.
Date Received
December 29, 1980
Decision Date
January 13, 1981
Product Code
DWE
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
DWE Tubing, Pump, Cardiopulmonary Bypass

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