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

BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO

K Number: K834048 · Decision Apr 4, 1984
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
21
Review Days
133

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Basic Information

Device Name
BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO
K Number
K834048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Castle Co.
Date Received
November 23, 1983
Decision Date
April 4, 1984
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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K833074 CASTLE TEC-TEST S.M.A.R.T. PACK
K831595 CASTLE MODEL 3341 & 3441 & 4141 GAS AER
K792660 1500 EO EXHAUST HOOD
K792649 UNISPORE-BIOLOGICAL INDICATORS
K790677 EO EVACUATING SYSTEM I
K781887 9100 DAYSTAR AND 9110 ORBITER PACKAGE
K781484 CASTLE MODEL 3146 GAS AERATOR
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