Atlas FDA

SteriHub™ Disinfecting Device and Protective Cover

FDA 510(k) clearance K251592 · decided 2026-02-11

Clearance details

K-number
K251592
Device name
SteriHub™ Disinfecting Device and Protective Cover
Applicant
1World Vista Medical
Decision
Substantially Equivalent
Date received
2025-05-23
Decision date
2026-02-11
Days to decision
264 days
Clearance type
Traditional
Product code
QBP
Device class
2
Regulation number
880.5440
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Rio Verde, AZ, 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
OTTO™ Disinfecting Cap (K252006)Icu Medical, Inc.2026-03-27
ACTIV™ Cap (K223914)Cleansite Medical, Inc.2024-04-05
BD PureHub Disinfecting Cap (K193190)Becton, Dickinson and Company2020-11-09
Curos Jet Disinfecting Cap (K200299)3M Company2020-10-29
CapKlenZ (K192382)Star Mountain Medical, Inc.2020-04-20
SwabTip Male Disinfectant Cap (K190918)Icu Medical2020-03-06
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.