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

ARRIRM SCRUB BRUSH/SPONGE

K Number: K823173 · Decision Nov 22, 1982
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
36
Applicant Total
18
Review Days
27

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Basic Information

Device Name
ARRIRM SCRUB BRUSH/SPONGE
K Number
K823173
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
The Buckeye Cellulose Corp.
Date Received
October 26, 1982
Decision Date
November 22, 1982
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 The Buckeye Cellulose Corp.

K Number Device Name
K822925 BOUNDARY SINGLE-USE GOWNS
K821564 BOUNDARY PROCESS CHANGE
K820758 BOUNDARY SINGLE-USE CRANIOTOMY SHEET
K820116 BOUNDARY
K813450 BOUNDARY SINGLE-USE DRAPES
K813390 BONDARY SINGLE-USE OR GOWN
K813277 BOUNDARY DRAPE TAPE
K813263 PATIENT UNDERPAD
K812962 BOUNDARY SURGICAL DRAPE
K812738 BOUNDARY PROCESS CHANGE
Search all 18 clearances from The Buckeye Cellulose Corp. →