510(k) K080563
- Device
- RUNTHROUGH NS EXTENSION WIRE
- Applicant
- TERUMO MEDICAL CORP.
- 510(k) number
- K080563
- Product code
- DQX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2008-03-20
- Date received
- 2008-02-28
- Regulation
- 870.1330
- Classification name
- Wire, Guide, Catheter
- Medical specialty
- Cardiovascular
- Review panel
- Cardiovascular
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- MARK UNTERREINER
- Address
- 950 Elkton Blvd. Elkton MD US 21921 21921
FDA Registration Numbers#
- 3010532612
- 1724474
- 3010432890
- 3006082230
- 3014977413
- 3010665433
- 3007146453
- 1016427
- 1221806
- 3009490946
- 3016678045
- 3030446844
- 3004519921
- 1222301
- 3013162291
- 2182269
- 3000247873
- 1649869
- 1225687
- 3014590708
- 3015489752
- 3006425876
- 3008061490
- 3042175841
- 3006283319
- 9617592
- 3009546466
- 3008439199
- 1028232
- 9680794
- 3004111573
- 3015910259
- 3012536737
- 1824619
- 2134244
- 3020778
- 3011564431
- 1056553
- 2011171
- 2518902
- 3009121749
- 2126666
- 3013750125
- 3013656790
- 3020968442
- 9616088
- 3024682301
- 3013764800
- 3030733800
- 1054811
- 9616684
- 3011137372
- 3008363989
- 3013943846
- 3019751610
- 3008627763
- 3018784828
- 1313046
- 3026317086
- 3013595987
- 1043214
- 3011050570
- 3002808486
- 9614279
- 3003084417
- 3008403546
- 2134812
- 3000268902
- 3003780911
- 3036802499
- 2248146
- 3014222368
- 3004784537
- 3014461810
- 3012154226
- 3017210488
- 3014716786
- 3002917664
- 2183870
- 2134265
Source Documents#
Other 510(k) Records For Product Code DQX #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K254137 | InQwire Amplatz Guide Wire | Merit Medical Ireland, Ltd. | 2026-05-22 |
| K260544 | FMD Peripheral Guide Wire F-14 Flex 6; FMD Peripheral Guide Wire F-14 Tapered 40; FMD Peripheral Guide Wire F-18 Flex SP; FMD Peripheral Guide Wire F-18 DP 25; FMD Peripheral Guide Wire F-18 Tapered 40 | FMD Co., Ltd. | 2026-03-20 |
| K253746 | Enroute 0.014'' Transcarotid Guidewire | Lake Region Medical | 2026-03-19 |
| K253262 | EmeryGlide™ (EG18008901) | Nano4imaging GmbH | 2026-03-06 |
| K253847 | Splashwire Hydrophilic Guide Wire (MSWSTD35150J3) | Merit Medical Ireland, Ltd. | 2026-01-31 |
| K251385 | 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) | Merit Medical Ireland, Ltd. | 2026-01-21 |
| K252674 | Solo Pace Fusion System (SOLOFUSE1) | Solo Pace, Inc. | 2026-01-09 |
| K251596 | Lunderquist Extra Stiff Wire Guide | William Cook Europe Aps | 2025-11-09 |
| K250203 | SureAx-Guide™ | Sureax Medical, LLC | 2025-10-17 |
| K250031 | Amplatzer Guidewire | ABBOTT MEDICAL | 2025-10-03 |
| K251181 | Splashwire Hydrophilic Guide Wire (MSWSTD35180J1O5); Splashwire Hydrophilic Guide Wire (MSWSTD35260J1O5); Splashwire Hydrophilic Guide Wire (MSWSTDA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35260LT); Splashwire Hydrophilic Guide Wire (MSWSTFA35150LT); Splashwire Hydrophilic Guide Wire (MSWSTFS38150LT) | Merit Medical Ireland, Ltd. | 2025-08-29 |
| K250552 | Hi-Torque Command 14 ST Guide Wire and Hi-Torque Command 14 MT Guide Wire | ABBOTT MEDICAL | 2025-07-25 |
| K250075 | Medtronic Stedi Extra Support Guidewire | Medtronic, Inc. | 2025-06-13 |
| K243733 | SION blue PLUS | Asahi Intecc Co., Ltd. | 2025-04-02 |
| K241962 | Crossloop | Asahi Intecc Co., Ltd. | 2025-03-27 |
Legacy Summary#
summary
FDA Review#
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