Pennine Connecting Tubing
FDA 510(k) K852859 · Pennine Medical , Ltd.
510(k) numberK852859
Submission
- Device name
- Pennine Connecting Tubing
- Applicant
- Pennine Medical , Ltd.
Stoughton, MA, US - Received
- July 5, 1985
- Decision date
- July 30, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Pennine Medical , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K854443 | O'Neil Urinary Catheter IntroducerKOD · Traditional | 01/08/1986SE |
| K852081 | Pennine Oxygen Link TubingBYX · Traditional | 06/14/1985SE |
| K844874 | Pennine Link YankauersGEA · Traditional | 06/06/1985SE |
| K844876 | Pennine Nelaton Catheters Sizes 5,6,8,10,12,14,16,GBX · Traditional | 06/05/1985SE |
| K852080 | Pennine Suction CathetersBSY · Traditional | 06/03/1985SE |
| K852079 | Pennine Derby YankauerBSY · Traditional | 06/03/1985SE |
| K844873 | Pennine Guedel Airway 00,0,1,2,3 & 4CAE · Traditional | 02/21/1985SE |
Questions and answers
When was Pennine Connecting Tubing cleared by the FDA?
Pennine Connecting Tubing (K852859) received a 510(k) decision of Substantially Equivalent on July 30, 1985, 25 days after the submission was received.