Atlas FDA

Pulmonary Cytology Brush

FDA 510(k) clearance K182927 · decided 2020-02-07

Clearance details

K-number
K182927
Device name
Pulmonary Cytology Brush
Applicant
Hobbs Medical, Inc.
Decision
Substantially Equivalent
Date received
2018-10-22
Decision date
2020-02-07
Days to decision
473 days
Clearance type
Traditional
Product code
BTG
Device class
2
Regulation number
874.4680
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Stafford Springs, CT, 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
Disposable Cytology Brush BC-202D/203D Series (K251279)Olympus Medical Systems Corporation2025-06-12
Single Use Cytology Brush BC-205D (K190293)Olympus Medical Systems Corp.2019-08-02
SUPERDIMENSION TRIPLE-NEEDLE CYTOLOGY BRUSH (K130357)Covidien, LLC2013-11-06
MICROBIOLOGY SPECIMEN BRUSH (K820771)Mill-Rose Laboratory1982-05-03
CYTOLOGY BRUSH (K780872)CooperVision, Inc.1978-09-07

Recalls involving this device

RecordFirmDate
Hobbs Medical Cytology Brush Catalog Number: 4204 recall (Z-0013-2023)Hobbs Medical, Inc.2022-10-07
Hobbs Medical Polypectomy Snare Catalog Number: 4563 recall (Z-0015-2023)Hobbs Medical, Inc.2022-10-07