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

MICROVASIVE SILICONE SPRAY

K Number: K854063 · Decision Oct 25, 1985
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
18
Review Days
21

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Basic Information

Device Name
MICROVASIVE SILICONE SPRAY
K Number
K854063
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Microvasive
Date Received
October 4, 1985
Decision Date
October 25, 1985
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Similar 510(k) Clearances

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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
K860366 CHALLENGER HOT BIOPSY FORCEPS
K854238 NEEDLE W/STYLET FOR IMPLANTATION
K851652 PAPILLOTOME
K850393 FLEXIBLE FIBEROPTIC ENDOSCOPE
K844769 RIGID FIBEROPITC ENDOSCOPE
Search all 18 clearances from Microvasive →