FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AP X-RAY TUBE ANGULATION DEVICE

K Number: K811970 · Decision Aug 13, 1981
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
39
Applicant Total
190
Review Days
34

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Basic Information

Device Name
AP X-RAY TUBE ANGULATION DEVICE
K Number
K811970
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1770
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Philips Medical Systems (Cleveland), Inc.
Date Received
July 10, 1981
Decision Date
August 13, 1981
Product Code
IYB
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
IYB Tube Mount, X-Ray, Diagnostic

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