IQMARK DIGITAL HOLTER— 510(k) K031466

Name: FDA 510(k) clearance K031466
Creator: U.S. Food and Drug Administration
Published: 2003-06-11

Substantially Equivalent

Brentwood Medical Technology Corp.

FDA 510(k) clearance K031466 for IQMARK DIGITAL HOLTER, Substantially Equivalent on 2003-06-11. Applicant: Brentwood Medical Technology Corp.. Device class: 2.

Clearance details

Applicant: Brentwood Medical Technology Corp.
Product code: Code MLO
Device class: Class 2
Regulation: 21 CFR 870.2800
Advisory panel: Cardiovascular
Date received: 2003-05-08
Decision date: 2003-06-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Torrance, CA, US

Download summary PDF View on FDA.gov ↗

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