MEDTEC AUTOBLOT 2000— 510(k) K951753

Substantially Equivalent

Medtec, Inc.

FDA 510(k) clearance K951753 for MEDTEC AUTOBLOT 2000, Substantially Equivalent on 1995-10-17. Applicant: Medtec, Inc.. Device class: 1.

Clearance details

Applicant: Medtec, Inc.
Product code: Code JQW
Device class: Class 1
Regulation: 21 CFR 862.2750
Advisory panel: Clinical Chemistry
Date received: 1995-04-17
Decision date: 1995-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.