Global Medical Products Tuohy & Crawford Epidural Needle W/Plastic Hub
FDA 510(k) K952275 · Global Medical Prods, Inc.
510(k) numberK952275
Submission
- Device name
- Global Medical Products Tuohy & Crawford Epidural Needle W/Plastic Hub
- Applicant
- Global Medical Prods, Inc.
Clearwater, FL, US - Received
- May 15, 1995
- Decision date
- October 11, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- BSP – Needle, Conduction, Anesthetic (W/Wo Introducer)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5150
- Specialty
- Anesthesiology
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| K241953 | SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyBSP · Traditional | PAJUNK GmbH Medizintechnologie | 11/22/2024SE |
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| K871556 | Merivaara Emergency Patient Trolley #436FPO · Traditional | 04/30/1987SE |
| K863748 | Hospital BedFNJ · Traditional | 10/09/1986SE |
| K862959 | Merivaara Patient Trolley - Model #416FPO · Traditional | 09/25/1986SE |
| K862957 | Merivaara Geriatric Chair Model 455INN · Traditional | 08/21/1986SE |
| K862931 | Merivaara Obstetric Chair/Bed-Model 358KNC · Traditional | 08/07/1986SE |
Questions and answers
When was Global Medical Products Tuohy & Crawford Epidural Needle W/Plastic Hub cleared by the FDA?
Global Medical Products Tuohy & Crawford Epidural Needle W/Plastic Hub (K952275) received a 510(k) decision of Substantially Equivalent on October 11, 1995, 149 days after the submission was received.
What is the product code of K952275?
The FDA product code is BSP – Needle, Conduction, Anesthetic (W/Wo Introducer), a Class II (moderate risk) device regulated under 21 CFR 868.5150.