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

NAMIC ANGIOGRAPHIC SYRINGE

K Number: K873955 · Decision Feb 5, 1988
Classifications
1
FEI Numbers
124
Registration Numbers
124
Same Product Code
209
Applicant Total
28
Review Days
130

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Basic Information

Device Name
NAMIC ANGIOGRAPHIC SYRINGE
K Number
K873955
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1650
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
North American Instrument Corp.
Date Received
September 28, 1987
Decision Date
February 5, 1988
Product Code
DXT
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
DXT Injector And Syringe, Angiographic

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Other Clearances by North American Instrument Corp.

K Number Device Name
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K922552 MORSE(R) ANGIOGRAPHIC CATHETERS
K915078 MORSE HEMOSTATIC CATHETER INTRODUCER SET
K905208 MORSE ANESTHESIA
K912961 MORSE VASCULAR INTRODUCER SET
K910764 THE PERCEPTOR(TM) STAND ALONE TRANSDUCER
K903493 NAMIC CONTRAST SAVINGS DELIVERY SYSTEM
K904275 MORSE BALLOON INFLATION DEVICE
Search all 28 clearances from North American Instrument Corp. →