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

SURGI-BRUSH

K Number: K896085 · Decision Nov 8, 1989
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
36
Applicant Total
7
Review Days
20

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Basic Information

Device Name
SURGI-BRUSH
K Number
K896085
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Sparta Surgical Corp.
Date Received
October 19, 1989
Decision Date
November 8, 1989
Product Code
GEC
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
GEC Brush, Scrub, Operating-Room

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Other Clearances by Sparta Surgical Corp.

K Number Device Name
K965187 SPECTRUM II, SPECTRUM PLUS, AND SPECTRUM MAX-SD
K945313 SPARTA HYDROGEL WOUND DRESSING
K922729 SPARTA WET DRESSING, SODIUM CHLORIDE
K905384 DAVID SIMMONDS ANESTHESIA EXTENSION TUBES
K905240 VESSELOOPS
K896084 MICROSPEARS