• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
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FDA 510(k) K142806, DualCap, by Catheter Connections, Inc.

FDA 510(k) K142806, DualCap, by Catheter Connections, Inc.

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510(K) Number: K142806
Device Name: DualCap
Manufacturer: Catheter Connections, Inc.
Device Classification Name: cap, device disinfectant
Regulation Number: 880.5440
Classification Product Code: QBP
Date Received: 09/29/2014
Decision Date: 05/22/2015
Regulation Medical Specialty: General Hospital

203 pages (371 of 574 original pages are fully redacted)
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