URESIL ENDOSCOPIC LASER OVERTUBE— 510(k) K901882

Substantially Equivalent

Uresil Corp.

FDA 510(k) clearance K901882 for URESIL ENDOSCOPIC LASER OVERTUBE, Substantially Equivalent on 1990-07-27. Applicant: Uresil Corp..

Clearance details

Applicant: Uresil Corp.
Product code: Code KOQ
Advisory panel: Dental
Date received: 1990-04-26
Decision date: 1990-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skokie, IL, US

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