K-number	K811967
Device name	CP-625 SEE-THRU FILM CHANGER
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	KPX
Device class	Class II
Decision date	Aug 13, 1981
Decision	Substantially Equivalent
Regulation	892.1860

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View the full FDA submission: accessdata.fda.gov

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CP-625 SEE-THRU FILM CHANGER

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