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

Name: FDA 510(k) clearance K881185
Creator: U.S. Food and Drug Administration
Published: 1988-06-01

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.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code HEM
Device class: Class 2
Regulation: 21 CFR 884.2225
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

Download summary PDF View on FDA.gov ↗

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