ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.— 510(k) K881185

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K881185 for ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA., Substantially Equivalent on 1988-06-01. Applicant: Philips Medical Systems (Cleveland), Inc..

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code HEM
Advisory panel: Obstetrics/Gynecology
Date received: 1988-03-21
Decision date: 1988-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

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