FIBER OPTIC ENDOILLUMINATION PROBE— 510(k) K980636

Substantially Equivalent

Dutch Ophthalmic USA, Inc.

FDA 510(k) clearance K980636 for FIBER OPTIC ENDOILLUMINATION PROBE, Substantially Equivalent on 1998-05-20. Applicant: Dutch Ophthalmic USA, Inc..

Clearance details

Applicant: Dutch Ophthalmic USA, Inc.
Product code: Code FFS
Advisory panel: Gastroenterology, Urology
Date received: 1998-02-19
Decision date: 1998-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kingston, NH, US

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