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

PERCUTANEOUS ANGIOGRAPHIC NEEDLES

K Number: K845037 · Decision Jun 21, 1985
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
92
Review Days
176

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Basic Information

Device Name
PERCUTANEOUS ANGIOGRAPHIC NEEDLES
K Number
K845037
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Mallinckrodt Critical Care
Date Received
December 27, 1984
Decision Date
June 21, 1985
Product Code
DYB
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
DYB Introducer, Catheter

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Other Clearances by Mallinckrodt Critical Care

K Number Device Name
K880343 BURNEY GALLBLADDER CATHETER KIT
K874605 HI-LO TEMP(R) MYOCARDIAL TEMPERATURE SENSOR
K874514 HI-LO TEMP(R) GENERAL PURPOSE TEMPERATURE PROBE
K874568 HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR
K874404 HI-LO TEMP(R) SKIN TEMPERATURE SENSOR
K873461 LASER-FLEX(TM) TRACHEAL TUBE (CUFFED)
K873833 THERMOCOUPLE ADAPTER
K873004 GUIDING CATHETER
K871204 CUFFED TRACHEAL TUBE (MULTIPLE)
K862666 UNCUFFED LASER RESISTEANT TRACHEAL TUBE(TENTATIVE)
Search all 92 clearances from Mallinckrodt Critical Care →