DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP— 510(k) K875024

Name: FDA 510(k) clearance K875024
Creator: U.S. Food and Drug Administration
Published: 1988-01-22

Substantially Equivalent

Dey Laboratories, Inc.

FDA 510(k) clearance K875024 for DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, Substantially Equivalent on 1988-01-22. Applicant: Dey Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Dey Laboratories, Inc.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1987-12-04
Decision date: 1988-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, CA, US

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