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510(k) K811967

CP-625 SEE-THRU FILM CHANGER by Philips Medical Systems (Cleveland), Inc. — Product Code KPX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 13, 1981
Date Received
July 10, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Changer, Radiographic Film/Cassette
Device Class
Class II
Regulation Number
892.1860
Review Panel
RA
Submission Type

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  • K905789 — FRANKLIN 9000 WALL STAND (May 20, 1991)