SALIVART

FDA Premarket Approval P790016

Pre-market Approval Supplement Details

• Device: SALIVART
• Generic Name: Saliva, Artificial
• Applicant: WESTPORT PHARMACEUTICALS, INC.
• Date Received: 1979-06-12
• Decision Date: 1979-09-19
• Notice Date: 1980-04-25
• PMA: P790016
• Supplement: S
• Product Code: LFD
• Docket Number: 80M-0058
• Advisory Committee: Dental
• Expedited Review: No
• Combination Product: No
• Applicant Address: WESTPORT PHARMACEUTICALS, INC. p.o. Box 5022 weston, CT 06881

Supplemental Filings

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Supplement Number	Date	Supplement Type
P790016		Original Filing