LITHOVAC SUCTION/ASPIRATION PROBE— 510(k) K964111

Substantially Equivalent

Electro Medical Systems SA

FDA 510(k) clearance K964111 for LITHOVAC SUCTION/ASPIRATION PROBE, Substantially Equivalent on 1996-12-16. Applicant: Electro Medical Systems SA. Device class: 2.

Clearance details

Applicant
Electro Medical Systems SA
Product code
Code KQT
Device class
Class 2
Regulation
21 CFR 876.4370
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
North Attleboro, MA, US
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