The following data is part of a premarket notification filed by Avid N.i.t., Inc. with the FDA for Avid-nit Nerve Stimulation Needles.
| Device ID | K014246 |
| 510k Number | K014246 |
| Device Name: | AVID-NIT NERVE STIMULATION NEEDLES |
| Classification | Anesthesia Conduction Kit |
| Applicant | AVID N.I.T., INC. 390 SCARLET BLVD. Oldsmar, FL 34677 |
| Contact | Scott Henderson |
| Correspondent | Scott Henderson AVID N.I.T., INC. 390 SCARLET BLVD. Oldsmar, FL 34677 |
| Product Code | CAZ |
| CFR Regulation Number | 868.5140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-12-26 |
| Decision Date | 2002-07-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30801902061172 | K014246 | 000 |
| 30801902061165 | K014246 | 000 |
| 30801902061158 | K014246 | 000 |
| 20801902061168 | K014246 | 000 |