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

ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL

K Number: K915731 · Decision Nov 5, 1992
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
26
Review Days
321

Basic Information

Device Name
ELECTROSURGICAL UNITS ESU 30, 70, 70 B, 70 DIGITAL
K Number
K915731
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ELMED, INC.
Date Received
December 20, 1991
Decision Date
November 5, 1992
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K932938 ELMED ESU 300 M/M AND DIGITAL
K921770 ELECTROSURGICAL UNITS ESU 100L, 100 L M/M & E M/M
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K881431 SIEMENS STEREODYNATOR 828
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