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.. Device class: 2.

Clearance details

Applicant: Dunn Instruments, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1977-10-13
Decision date: 1977-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Dunn Instruments, Inc.

K850184 — MEDICAL MULTI-IMAGE CAMERA-6761985-02-21
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Data sourced from openFDA. This site is unofficial and independent of the FDA.