VIVONEX MASS GASTRASTOMY TUBE— 510(k) K822516

Name: FDA 510(k) clearance K822516
Creator: U.S. Food and Drug Administration
Published: 1982-09-07

Substantially Equivalent

Norwich Eaton Pharmaceuticals, Inc.

FDA 510(k) clearance K822516 for VIVONEX MASS GASTRASTOMY TUBE, Substantially Equivalent on 1982-09-07. Applicant: Norwich Eaton Pharmaceuticals, Inc.. Device class: 1.

Clearance details

Applicant: Norwich Eaton Pharmaceuticals, Inc.
Product code: Code KHT
Device class: Class 1
Regulation: 21 CFR 866.5370
Advisory panel: Immunology
Date received: 1982-08-20
Decision date: 1982-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K831971 — VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE1983-09-01
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