FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LITHOVAC SUCTION/ASPIRATION PROBE

K Number: K964111 · Decision Dec 16, 1996
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
13
Applicant Total
9
Review Days
62

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Basic Information

Device Name
LITHOVAC SUCTION/ASPIRATION PROBE
K Number
K964111
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4370
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Electro Medical Systems SA
Date Received
October 15, 1996
Decision Date
December 16, 1996
Product Code
KQT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KQT Evacuator, Gastro-Urology

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Other Clearances by Electro Medical Systems SA

K Number Device Name
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K022119 EMS AIR-FLOW HANDY 2 DENTAL HANDPIECE
K012445 EMS SWISS LITHOCLAST MASTER (A.K.A. SWISS LITHOCLAST ULTRA)
K002484 EMS SWISS ORTHOCLAST CHISELS FOR NON-CEMENTED PROSTHESIS REMOVAL
K992251 SWISS LITHOCLAST MULTIPURPOSE PROBE
K963285 EMS SWISS LITHOCLAST LITHOTRIPTER
K953026 MINIPIEZON
K951531 SWISS LITHOCLAST LITHOTRIPTER