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

JEJUNAL FEEDING TUBE

K Number: K861309 · Decision Dec 16, 1986
Classifications
1
FEI Numbers
228
Registration Numbers
229
Same Product Code
648
Applicant Total
18
Review Days
252

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Basic Information

Device Name
JEJUNAL FEEDING TUBE
K Number
K861309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Microvasive
Date Received
April 8, 1986
Decision Date
December 16, 1986
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNT), 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
K861323 REPLACEMENT GASTROSTOMY TUBE
K860589 INFLATOR/DEFLATOR PISTON SYRINGE
K860366 CHALLENGER HOT BIOPSY FORCEPS
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 →