SENTINEL RECORDER, MODELS 471/472— 510(k) K971696

Name: FDA 510(k) clearance K971696
Creator: U.S. Food and Drug Administration
Published: 1997-12-30

Substantially Equivalent

Del Mar Avionics

FDA 510(k) clearance K971696 for SENTINEL RECORDER, MODELS 471/472, Substantially Equivalent on 1997-12-30. Applicant: Del Mar Avionics. Device class: 2.

Clearance details

Applicant: Del Mar Avionics
Product code: Code DXH
Device class: Class 2
Regulation: 21 CFR 870.2920
Advisory panel: Cardiovascular
Date received: 1997-05-08
Decision date: 1997-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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