Atlas FDA

DEFLECTING CYTOLOGY BRUSH

FDA 510(k) clearance K822490 · decided 1982-09-14

Clearance details

K-number
K822490
Device name
DEFLECTING CYTOLOGY BRUSH
Applicant
Van-Tec, Inc.
Decision
Substantially Equivalent
Date received
1982-08-18
Decision date
1982-09-14
Days to decision
27 days
Clearance type
Traditional
Product code
GEE
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
STERILE SOFT TISSUE BIOPSY NEEDLE (K854003)Co-Medical, Inc.1985-10-18
BIOPSY PUNCH, VARIOUS (K841008)Premier Dental Products Co.1984-06-08
STERILE CYTOLOGY BRUSHES (K820259)American Endoscopy, Inc.1982-03-05
WHISK-R (K812694)Medi-Spec1981-10-26
CAMLOC SYRINGE BIOPSY KIT (K801304)Johannah Medical Services, Inc.1980-06-17
TROTEX II SCREW NEEDLE BIOPSY INSTR. SET (K792316)Ursus Konsult AB1979-12-18

Recalls involving this device

No recalls on record reference this clearance.