MODIFIED SEISMOCARDIOGRAPH— 510(k) K900130

Substantially Equivalent

Seismed Instruments, Inc.

FDA 510(k) clearance K900130 for MODIFIED SEISMOCARDIOGRAPH, Substantially Equivalent on 1990-03-28. Applicant: Seismed Instruments, Inc..

Clearance details

Applicant: Seismed Instruments, Inc.
Product code: Code DSB
Advisory panel: Cardiovascular
Date received: 1990-01-05
Decision date: 1990-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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