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

INSTRUMENT CLEANING BRUSH

K Number: K780399 · Decision Mar 17, 1978
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
7
Review Days
4

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Basic Information

Device Name
INSTRUMENT CLEANING BRUSH
K Number
K780399
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Ransom and Randolph
Date Received
March 13, 1978
Decision Date
March 17, 1978
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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K770598 ENDODONTIC INSTRUMENTS, R&R CUTWELL
K761067 DENTSPLY DIE STONE