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

MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE

K Number: K883174 · Decision Oct 14, 1988
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
503
Review Days
79

Basic Information

Device Name
MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE
K Number
K883174
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
BAXTER HEALTHCARE CORP.
Date Received
July 27, 1988
Decision Date
October 14, 1988
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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