FDA 510(k), K142806, DualCap

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)