LABELLING MODIFICATION TO MAXX PLUS— 510(k) K904453

Substantially Equivalent

Mayer Laboratories

FDA 510(k) clearance K904453 for LABELLING MODIFICATION TO MAXX PLUS, Substantially Equivalent on 1990-11-23. Applicant: Mayer Laboratories.

Clearance details

Applicant: Mayer Laboratories
Product code: Code HIS
Advisory panel: Obstetrics/Gynecology
Date received: 1990-09-27
Decision date: 1990-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oakland, CA, US

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