ACA DU PONT METHOTREXATE (MTHO) METHOD— 510(k) K884744

Name: FDA 510(k) clearance K884744
Creator: U.S. Food and Drug Administration
Published: 1989-01-30

Substantially Equivalent

E.I. Dupont DE Nemours & Co., Inc.

FDA 510(k) clearance K884744 for ACA DU PONT METHOTREXATE (MTHO) METHOD, Substantially Equivalent on 1989-01-30. Applicant: E.I. Dupont DE Nemours & Co., Inc.. Device class: Unclassified.

Clearance details

Applicant: E.I. Dupont DE Nemours & Co., Inc.
Product code: Code LAO
Device class: Unclassified
Advisory panel: Unknown
Date received: 1988-11-14
Decision date: 1989-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

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