DURALIFE(TM)— 510(k) K913726

Substantially Equivalent

Dhd Diemolding Healthcare Div.

FDA 510(k) clearance K913726 for DURALIFE(TM), Substantially Equivalent on 1992-02-07. Applicant: Dhd Diemolding Healthcare Div.. Device class: 1.

Clearance details

Applicant: Dhd Diemolding Healthcare Div.
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
Advisory panel: Anesthesiology
Date received: 1991-08-20
Decision date: 1992-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canastota, NY, US

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