MEGA AMNIOCENTESIS KIT— 510(k) K915863

Unknown

Mega Medical, Inc.

FDA 510(k) clearance K915863 for MEGA AMNIOCENTESIS KIT, Unknown on 1992-03-30. Applicant: Mega Medical, Inc..

Clearance details

Applicant: Mega Medical, Inc.
Product code: Code HIO
Advisory panel: Obstetrics/Gynecology
Date received: 1991-12-31
Decision date: 1992-03-30
Decision: Unknown
Clearance type: Traditional
Location: Tampa, FL, US

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