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

STERILE CYTOLOGY BRUSHES

K Number: K820259 · Decision Mar 5, 1982
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
6
Applicant Total
19
Review Days
32

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Basic Information

Device Name
STERILE CYTOLOGY BRUSHES
K Number
K820259
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
American Endoscopy, Inc.
Date Received
February 1, 1982
Decision Date
March 5, 1982
Product Code
GEE
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
GEE Brush, Biopsy, General & Plastic Surgery

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K833859 TAMPONADE BALLOON CUFF
K833492 PERCUTANEOUS ENDOSCOPIC GASTROSCOPY
K832458 AUTOMATIC ENDOSCOPE
K821818 RETRIEVAL BALLOONS
K821819 PIGTAIL STENTS
K822062 BALL TIP COAGULATING ELECTRODES
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