K022029 is an FDA 510(k) clearance for the QUINCKE SPINAL NEEDLE. This device is classified as a Needle, Conduction, Anesthetic (w/wo Introducer) (Class II - Special Controls, product code BSP).
Submitted by Epimed International, Inc. (Johnstown, US). The FDA issued a Cleared decision on July 30, 2002, 39 days after receiving the submission on June 21, 2002.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5150.
| 510(k) Number | K022029 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 21, 2002 |
| Decision Date | July 30, 2002 |
| Days to Decision | 39 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BSP — Needle, Conduction, Anesthetic (w/wo Introducer) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5150 |