Atlas FDA

BD PureHub Disinfecting Cap

FDA 510(k) clearance K193190 · decided 2020-11-09

Clearance details

K-number
K193190
Device name
BD PureHub Disinfecting Cap
Applicant
Becton, Dickinson and Company
Decision
Substantially Equivalent
Date received
2019-11-19
Decision date
2020-11-09
Days to decision
356 days
Clearance type
Traditional
Product code
QBP
Device class
2
Regulation number
880.5440
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Franklin Lakes, NJ, US
Third-party review
No
Expedited review
No

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OTTO™ Disinfecting Cap (K252006)Icu Medical, Inc.2026-03-27
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DualCap (K142806)Catheter Connections, Inc.2015-05-22
CUROS RED PORT PROTECTOR (K140657)Ivera Medical, Inc.2014-12-04
DualCap IV Pole Strips(Disinfectant Caps for Male Luers) (K142399)Catheter Connections, Inc.2014-11-19
SWABCAP AND SWABFLUSH (K130975)Excelsior Medical Corp.2013-12-24
CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS (K123967)Catheter Connections, Inc.2013-01-22
CATHETER CONNECTIONS DUALCAP SOLO (K123065)Catheter Connections, Inc.2012-12-14

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BD ONCLARITY HPV ASSAY (P160037/S022)Becton, Dickinson and Company2025-08-25
BD Onclarity HPV Assay (P160037/S023)Becton, Dickinson and Company2025-07-02
Onclarity HPV Assay (P160037/S021)Becton, Dickinson and Company2025-03-12
BD Onclarity™ HPV Assay (P160037/S020)Becton, Dickinson and Company2024-11-05
BD Onclarity HPV Assay (P160037/S017)Becton, Dickinson and Company2024-05-14
BD Onclarity™ HPV Assay (P160037/S019)Becton, Dickinson and Company2024-04-18
BD Onclarity HPV Assay (P160037/S018)Becton, Dickinson and Company2023-11-20
BD Onclarity HPV (P160037/S016)Becton, Dickinson and Company2023-11-15