510(k) K251385
- Device
- InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S)
- Applicant
- Merit Medical Ireland, Ltd.
- 510(k) number
- K251385
- Product code
- DQX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2026-01-21
- Date received
- 2025-05-05
- Regulation
- 870.1330
- Classification name
- Wire, Guide, Catheter
- Medical specialty
- Cardiovascular
- Review panel
- Cardiovascular
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Shane Costello
- Address
- Parkmore Business Park W. Galway IE
FDA Registration Numbers
- 3010665433
- 1450662
- 3014499739
- 2184149
- 2133928
- 2248146
- 2521402
- 3003289691
- 3012050423
- 9617592
- 1061124
- 9616662
- 3018784828
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- 3030446844
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- 2124215
- 9680001
- 2135147
- 2024311
- 3014162263
- 3012179728
- 3000268902
- 1282497
- 3008837339
- 3012223769
- 2518902
- 3003790304
- 1313046
- 3015522130
- 1221806
- 3010419931
- 3015489752
- 1226348
- 3010041511
- 9610849
- 1054241
- 1319211
- 2527072
- 2134285
- 3004748528
- 1064858
- 3007146453
- 9680794
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- 3024743081
- 3016678045
- 3030574705
- 2029214
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- 2528981
- 3003775027
- 3014461810
- 3009600098
- 3009546466
- 1016427
- 3020954746
- 3014977413
- 3009564766
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
Other 510(k) Records For Product Code DQX
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