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

NEUROLOGICAL SPONGE

K Number: K914600 · Decision Dec 30, 1992
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
23
Applicant Total
41
Review Days
446

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Basic Information

Device Name
NEUROLOGICAL SPONGE
K Number
K914600
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4700
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
I M, Inc.
Date Received
October 11, 1991
Decision Date
December 30, 1992
Product Code
HBA
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HBA Neurosurgical Paddie

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Other Clearances by I M, Inc.

K Number Device Name
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
K853286 STAPLE REMOVER
Search all 41 clearances from I M, Inc. →