The following data is part of a premarket notification filed by Incutech, Inc. with the FDA for More-l Injector Kit Plus.
| Device ID | K960619 |
| 510k Number | K960619 |
| Device Name: | MORE-L INJECTOR KIT PLUS |
| Classification | Anesthesia Conduction Kit |
| Applicant | INCUTECH, INC. 307-A SOUTH WESTGATE DR. Greensboro, NC 27407 |
| Contact | Roger Molina |
| Correspondent | Roger Molina INCUTECH, INC. 307-A SOUTH WESTGATE DR. Greensboro, NC 27407 |
| Product Code | CAZ |
| CFR Regulation Number | 868.5140 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-02-13 |
| Decision Date | 1996-06-20 |