510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780872Substantially Equivalent

Cytology Brush

CooperVision, Inc., Southampton, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780872 is the FDA 510(k) clearance record for CYTOLOGY BRUSH, a class II device, cleared for CooperVision, Inc. on under FDA product code BTG (Brush, Biopsy, Bronchoscope (Non-Rigid)). FDA's definition for product code BTG reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 97 510(k) clearances for CooperVision, Inc., from to . As of , FDA records show 2 recalls naming K780872.

Clearance record

Decision date
Received
(100 days to decision)
Product code
BTG Brush, Biopsy, Bronchoscope (Non-Rigid)
Regulation
21 CFR 874.4680
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
CooperVision, Inc. Permalens House, Southampton, GB
Third party review
No

Clearances, product code BTG

Trailing 12 months

FDA records hold no clearances under product code BTG in the trailing twelve months.

FDA records show no clearances under product code BTG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BTG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260