SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL— 510(k) K950822

Name: FDA 510(k) clearance K950822
Creator: U.S. Food and Drug Administration
Published: 1995-03-22

Substantially Equivalent

Solopak Laboratories, Inc.

FDA 510(k) clearance K950822 for SOLOPAK PHARMACEUTICALS INC. STERILE EMPTY VIAL, Substantially Equivalent on 1995-03-22. Applicant: Solopak Laboratories, Inc..

Clearance details

Applicant: Solopak Laboratories, Inc.
Product code: Code LDH
Advisory panel: Unknown
Date received: 1995-02-22
Decision date: 1995-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elk Grove Village, IL, US

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