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

YESNG PATIENT PLATE #80226

K Number: K881144 · Decision Apr 8, 1988
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
35
Applicant Total
57
Review Days
22

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Basic Information

Device Name
YESNG PATIENT PLATE #80226
K Number
K881144
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ferguson Medical
Date Received
March 17, 1988
Decision Date
April 8, 1988
Product Code
JOS
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
JOS Electrode, Electrosurgical

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