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

SYRINGE

K Number: K833399 · Decision Jan 10, 1984
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
41
Review Days
97

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Basic Information

Device Name
SYRINGE
K Number
K833399
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
I M, Inc.
Date Received
October 5, 1983
Decision Date
January 10, 1984
Product Code
FMF
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
FMF Syringe, Piston

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Other Clearances by I M, Inc.

K Number Device Name
K914600 NEUROLOGICAL SPONGE
K892389 BIOPSY KIT
K881363 SYRINGE PREFILLED WITH WATER
K880753 UMBILICAL CORD CLAMP
K872741 NUTRIPUMP
K871495 BANDAGES CATALOG NUMBER: 101 TO 220
K863785 MAKLER CATHETER
K854155 STERILE SALINE SOLUTION
K853287 HUBOUT
K853288 FEEDING UNITS & TUBES
Search all 41 clearances from I M, Inc. →