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

PULSE GUARD ELECTRODE

K Number: K925396 · Decision Jul 30, 1993
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
60
Applicant Total
55
Review Days
277

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Basic Information

Device Name
PULSE GUARD ELECTRODE
K Number
K925396
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4480
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Northgate Technologies, Inc.
Date Received
October 26, 1992
Decision Date
July 30, 1993
Product Code
FFK
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
FFK Lithotriptor, Electro-Hydraulic

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K010053 HUMI-FLOW, MODEL 6-850-00/ 01/02
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