K-number	K881185
Device name	ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	HEM
Device class	Class II
Decision date	Jun 1, 1988
Decision	Substantially Equivalent
Regulation	884.2225

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View the full FDA submission: accessdata.fda.gov

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ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.

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