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

CHALLENGER HOT BIOPSY FORCEPS

K Number: K860366 · Decision Apr 7, 1986
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
187
Applicant Total
18
Review Days
63

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Basic Information

Device Name
CHALLENGER HOT BIOPSY FORCEPS
K Number
K860366
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Microvasive
Date Received
February 3, 1986
Decision Date
April 7, 1986
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)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNS), ordered by most recent decision date.

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Other Clearances by Microvasive

K Number Device Name
K872771 LOW PROFILE GASTROSTOMY
K870705 THERMAL COAGULATOR
K861309 JEJUNAL FEEDING TUBE
K861323 REPLACEMENT GASTROSTOMY TUBE
K860589 INFLATOR/DEFLATOR PISTON SYRINGE
K854238 NEEDLE W/STYLET FOR IMPLANTATION
K854063 MICROVASIVE SILICONE SPRAY
K851652 PAPILLOTOME
K850393 FLEXIBLE FIBEROPTIC ENDOSCOPE
K844769 RIGID FIBEROPITC ENDOSCOPE
Search all 18 clearances from Microvasive →