ELECTRODE, DISPERSIVE, DISP. NEOPAD— 510(k) K780118

Name: FDA 510(k) clearance K780118
Creator: U.S. Food and Drug Administration
Published: 1978-02-23

Substantially Equivalent

Neomed Corp.

FDA 510(k) clearance K780118 for ELECTRODE, DISPERSIVE, DISP. NEOPAD, Substantially Equivalent on 1978-02-23. Applicant: Neomed Corp.. Device class: 2.

Clearance details

Applicant: Neomed Corp.
Product code: Code HAM
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1978-01-23
Decision date: 1978-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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