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

ELECTROSURGICAL UNIT

K Number: K780293 · Decision Mar 14, 1978
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
30
Applicant Total
10
Review Days
21

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Basic Information

Device Name
ELECTROSURGICAL UNIT
K Number
K780293
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ritter Co.
Date Received
February 21, 1978
Decision Date
March 14, 1978
Product Code
HAM
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
HAM Apparatus, Electrosurgical

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