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

BALL TIP COAGULATING ELECTRODES

K Number: K822062 · Decision Aug 19, 1982
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
19
Review Days
37

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Basic Information

Device Name
BALL TIP COAGULATING ELECTRODES
K Number
K822062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American Endoscopy, Inc.
Date Received
July 13, 1982
Decision Date
August 19, 1982
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 American Endoscopy, Inc.

K Number Device Name
K853274 AMERICAN DILATATION SYSTEM
K841384 PROXIMA 1 PH MONITOR
K833491 ENDO BITE BLOCK
K840818 BIOPSY FORCEPS
K833859 TAMPONADE BALLOON CUFF
K833492 PERCUTANEOUS ENDOSCOPIC GASTROSCOPY
K832458 AUTOMATIC ENDOSCOPE
K821818 RETRIEVAL BALLOONS
K821819 PIGTAIL STENTS
K821817 PIGTAIL NASAL CATHETERS
Search all 19 clearances from American Endoscopy, Inc. →