DHD EMERALD PRODUCT— 510(k) K970596

Name: FDA 510(k) clearance K970596
Creator: U.S. Food and Drug Administration
Published: 1997-05-16

Substantially Equivalent

Dhd Diemolding Healthcare Div.

FDA 510(k) clearance K970596 for DHD EMERALD PRODUCT, Substantially Equivalent on 1997-05-16. Applicant: Dhd Diemolding Healthcare Div.. Device class: 2.

Clearance details

Applicant: Dhd Diemolding Healthcare Div.
Product code: Code BWF
Device class: Class 2
Regulation: 21 CFR 868.5690
Advisory panel: Anesthesiology
Date received: 1997-02-18
Decision date: 1997-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wampsville, NY, 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.