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

CONCEPT SUCTION COAGULATOR

K Number: K800321 · Decision Feb 28, 1980
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
83
Review Days
16

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Basic Information

Device Name
CONCEPT SUCTION COAGULATOR
K Number
K800321
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
February 12, 1980
Decision Date
February 28, 1980
Product Code
KNS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

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K894929 STAPLE FIXATION SYSTEM
K892376 INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)
K891109 PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE
K881954 CONCEPT POWER SYSTEM
K884255 CONCEPT CCT-5200, THERMAL THERAPY SYSTEM
K882121 C-FLO SUCTION TUBE
K880414 TENDON HARVESTER
Search all 83 clearances from Concept, Inc. →