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

SPECIMEN TRAP

K Number: K834467 · Decision Feb 17, 1984
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
8
Applicant Total
18
Review Days
59

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Basic Information

Device Name
SPECIMEN TRAP
K Number
K834467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Microvasive
Date Received
December 20, 1983
Decision Date
February 17, 1984
Product Code
BYZ
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
BYZ Trap, Sterile Specimen

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Other Clearances by Microvasive

K Number Device Name
K872771 LOW PROFILE GASTROSTOMY
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K861309 JEJUNAL FEEDING TUBE
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
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