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

BOVIE MODEL X-10, X-10I, ELECTROSURGICAL GENERATOR

K Number: K910663 · Decision May 9, 1991
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
22
Review Days
84

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Basic Information

Device Name
BOVIE MODEL X-10, X-10I, ELECTROSURGICAL GENERATOR
K Number
K910663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Mdt Corp., Inc.
Date Received
February 14, 1991
Decision Date
May 9, 1991
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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Other Clearances by Mdt Corp., Inc.

K Number Device Name
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K942486 IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLE
K924380 MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVE
K926081 DENTAL LIGHT
K924955 MDT/HARVEY MC-8 AND MC-10
K932094 BOVIE ULTRASONIC SURGICAL ASPIRATOR
K931169 MDT DENTAL CHAIR
K920930 MDT/CASTLE 10/90 DUAL LOAD STATION
K922212 MDT CASTLE BIOSIGN TEST PACK
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