• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
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FDA 510(k) K780872, CYTOLOGY BRUSH, by CooperVision, Inc.

FDA 510(k) K780872, CYTOLOGY BRUSH, by CooperVision, Inc.

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510(K) Number: K780872
Device Name: CYTOLOGY BRUSH
Manufacturer: CooperVision, Inc.
Device Classification Name: brush, biopsy, bronchoscope (non-rigid)
Regulation Number: 874.4680
Classification Product Code: BTG
Date Received: 05/30/1978
Decision Date: 09/07/1978
Regulation Medical Specialty: Ear Nose & Throat
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