K030562 is an FDA 510(k) clearance for the TUOHY EPIDURAL 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 April 3, 2003, 41 days after receiving the submission on February 21, 2003.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5150.
| 510(k) Number | K030562 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 21, 2003 |
| Decision Date | April 03, 2003 |
| Days to Decision | 41 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 |