KALLESTAD ANTISERA TO PHENYTOIN— 510(k) K811775

Substantially Equivalent

Kallestad Laboratories, Inc.

FDA 510(k) clearance K811775 for KALLESTAD ANTISERA TO PHENYTOIN, Substantially Equivalent on 1981-07-10. Applicant: Kallestad Laboratories, Inc..

Clearance details

Applicant: Kallestad Laboratories, Inc.
Product code: Code DLP
Advisory panel: Clinical Toxicology
Date received: 1981-06-23
Decision date: 1981-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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