The following data is part of a premarket notification filed by Avid N.i.t., Inc. with the FDA for Aldrete Epidural Needle Without Introducer.
| Device ID | K972595 |
| 510k Number | K972595 |
| Device Name: | ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER |
| Classification | Needle, Conduction, Anesthetic (w/wo Introducer) |
| Applicant | AVID N.I.T., INC. 917 KLOSTERMAN RD. EAST Tarpon Springs, FL 34689 |
| Contact | Joseph E Harms |
| Correspondent | Joseph E Harms AVID N.I.T., INC. 917 KLOSTERMAN RD. EAST Tarpon Springs, FL 34689 |
| Product Code | BSP |
| CFR Regulation Number | 868.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-07-11 |
| Decision Date | 1998-05-20 |