The following data is part of a premarket notification filed by Diatek, Inc. with the FDA for Martin Trach-secure.
| Device ID | K810575 |
| 510k Number | K810575 |
| Device Name: | MARTIN TRACH-SECURE |
| Classification | Tube, Tracheostomy (w/wo Connector) |
| Applicant | DIATEK, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTO |
| CFR Regulation Number | 868.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-03-03 |
| Decision Date | 1981-03-17 |