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

RADIOPAQUE RULER

K Number: K902606 · Decision Sep 27, 1990
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
19
Review Days
107

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Basic Information

Device Name
RADIOPAQUE RULER
K Number
K902606
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Professional Medical Services
Date Received
June 12, 1990
Decision Date
September 27, 1990
Product Code
KPR
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KPR System, X-Ray, Stationary

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K904508 CONDOR ANALOG INFLATION SYRINGE
K904954 CONDOR DIGITAL INFLATION SYRINGE
K884577 PROCEDURE READY TRAYS
K890471 PMS ANGIO DRAPE
K884497 CONTROL SYRINGE
K872448 BLOOD CONTAINMENT PACK
K864555 3 RING ATTACHMENT
K854941 PMS PERCUTANEOUS PUNCTURE NEEDLE
Search all 19 clearances from Professional Medical Services →