ORIGINEEDLE, MODIFICATION— 510(k) K913816

Substantially Equivalent

Origin Medsystems, Inc.

FDA 510(k) clearance K913816 for ORIGINEEDLE, MODIFICATION, Substantially Equivalent on 1991-11-08. Applicant: Origin Medsystems, Inc..

Clearance details

Applicant: Origin Medsystems, Inc.
Product code: Code FHO
Advisory panel: Gastroenterology, Urology
Date received: 1991-08-26
Decision date: 1991-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Mateo, CA, US

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