NDM DIATEMP INFANT ELECTROSURG. DISP. P.— 510(k) K810920

Name: FDA 510(k) clearance K810920
Creator: U.S. Food and Drug Administration
Published: 1981-05-01

Substantially Equivalent

Ndm Corp.

FDA 510(k) clearance K810920 for NDM DIATEMP INFANT ELECTROSURG. DISP. P., Substantially Equivalent on 1981-05-01. Applicant: Ndm Corp.. Device class: 2.

Clearance details

Applicant: Ndm Corp.
Product code: Code HAM
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1981-04-06
Decision date: 1981-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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