FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DISPOSABLE SCALPELS

K Number: K831798 · Decision Jul 19, 1983
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
41
Review Days
46

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Basic Information

Device Name
DISPOSABLE SCALPELS
K Number
K831798
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
I M, Inc.
Date Received
June 3, 1983
Decision Date
July 19, 1983
Product Code
KDC
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
KDC Instrument, Surgical, Disposable

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K Number Device Name
K914600 NEUROLOGICAL SPONGE
K892389 BIOPSY KIT
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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
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