HEARTBEATER— 510(k) K771924

Substantially Equivalent

Dunn Instruments, Inc.

FDA 510(k) clearance K771924 for HEARTBEATER, Substantially Equivalent on 1977-11-28. Applicant: Dunn Instruments, Inc..

Clearance details

Applicant: Dunn Instruments, Inc.
Product code: Code DXG
Advisory panel: Cardiovascular
Date received: 1977-10-13
Decision date: 1977-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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