VIVONEX MASS GASTRASTOMY TUBE— 510(k) K822516

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..

Clearance details

Applicant: Norwich Eaton Pharmaceuticals, Inc.
Product code: Code KHT
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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