A10 ULTRASCOPE RECORDER— 510(k) K890142

Substantially Equivalent

Ems Medical, Inc.

FDA 510(k) clearance K890142 for A10 ULTRASCOPE RECORDER, Substantially Equivalent on 1989-02-06. Applicant: Ems Medical, Inc.. Device class: 1.

Clearance details

Applicant: Ems Medical, Inc.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1989-01-13
Decision date: 1989-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Livermore, CA, US

Download summary PDF View on FDA.gov ↗

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