FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

BIOPSY KIT

K Number: K892389 · Decision Jul 17, 1989
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
41
Review Days
101

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Basic Information

Device Name
BIOPSY KIT
K Number
K892389
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Applicant
I M, Inc.
Date Received
April 7, 1989
Decision Date
July 17, 1989
Product Code
LRO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRO General Surgery Tray

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Other Clearances by I M, Inc.

K Number Device Name
K914600 NEUROLOGICAL SPONGE
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
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