510(k) K834227
- Device
- DESERET SUBCLAVIAN JUGULAR CATH. SET
- Applicant
- PARKE-DAVIS CO.
- 510(k) number
- K834227
- Product code
- FOZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-03-19
- Date received
- 1983-12-06
- Regulation
- 880.5200
- Classification name
- Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 9610849
- 8021545
- 9610825
- 3015997711
- 1721676
- 3004129394
- 3015859709
- 1319211
- 9610847
- 1056186
- 3008496528
- 3004187702
- 3013298431
- 3010413216
- 3030446844
- 3014579161
- 3007616112
- 3015058854
- 2518902
- 3010384323
- 9616157
- 3010419931
- 3009888344
- 3016727301
- 3013162291
- 8043983
- 3004784537
- 3009750712
- 3030626857
- 9680091
- 3032916632
- 3015173212
- 3040153768
- 3021570645
- 3030733800
- 3011088743
- 9617592
- 3005941719
- 3004134316
- 9615908
- 2243072
- 1282497
- 2024311
- 2648045
- 3005246939
- 2029015
- 3018507299
- 1223004
- 1055236
- 9616088
- 9612126
- 9610987
- 8041187
- 3031233007
- 3035111606
- 8020785
- 3010934635
- 3002806603
- 3012809732
- 3002807314
- 3006846316
- 9616991
- 3012542015
- 9612433
- 1061124
- 3009758019
- 3001124136
- 3000247873
- 1043214
- 3010532612
- 9681835
- 1220905
- 3003916417
- 3007207906
- 1018470
- 3012421607
- 2246552
- 3017509841
- 1410248
- 3012039263
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FOZ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K260432 | Ruby Intravascular Catheter | Venocare, Inc. | 2026-09-02 |
| K260165 | Unimpregnated Central Venous Catheter | Spectrum Vascular | 2026-08-10 |
| K261041 | ClearSafe Closed System | MedSource Labs, LLC | 2026-07-10 |
| K260539 | MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV Catheter | MedSource Labs, LLC | 2026-07-09 |
| K253235 | Introcan Safety® Deep Access XL IV Catheter | B.Braun Medical, Inc. | 2026-05-15 |
| K252137 | BD Insyte™ IV Catheter | Becton Dickinson Infusion Therapy Systems, Inc. | 2026-04-02 |
| K252513 | Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm; 22G x 45mm; 24G x 32mm; 24G x 14mm, 26G x 14mm); Polywin Safety Adva (20G x 45mm; 22G x 64mm; 22G x 45mm ; 24G x 32 mm; 24G x 14mm; 14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm, 26G x 14mm) | Poly Medicure Limited | 2026-04-01 |
| K252398 | SURFLO Hybria Closed System Safety IV Catheter | Terumo Medical Products (Hangzhou) Co., Ltd. | 2025-12-17 |
| K252677 | Polyshield Safety IV Catheters | Poly Medicure Limited | 2025-11-05 |
| K251422 | BD Saf-T-Intima™ Subcutaneous Catheter System | Becton Dickinson Infusion Therapy Systems, Inc. | 2025-10-08 |
| K243403 | BD Nexiva™ Closed IV Catheter System | Becton Dickinson Infusion Therapy Systems, Inc. | 2025-07-25 |
| K251155 | BD Cathena™ Safety IV Catheter | Becton Dickinson Infusion Therapy Systems, Inc. | 2025-07-11 |
| K251654 | BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV Catheter and BD Insyte™ Autoguard™ BC Pro Shielded IV Catheter | Becton Dickinson Infusion Therapy Systems, Inc. | 2025-06-27 |
| K250682 | BD Nexiva™ Diffusics™ Closed IV Catheter System and BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector | Becton Dickinson Infusion Therapy Systems, Inc. | 2025-06-03 |
| K243105 | Ruby Intravascular Catheter | Venocare, Inc. | 2025-05-16 |
Legacy Summary#
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FDA Review#
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