The following data is part of a premarket notification filed by Medtec, Inc. with the FDA for Green Tec-2100.
| Device ID | K955236 |
| 510k Number | K955236 |
| Device Name: | GREEN TEC-2100 |
| Classification | Monitor, Patient Position, Light-beam |
| Applicant | MEDTEC, INC. P.O. BOX 487 1401 8TH STREET SOUTH EAST Orange City, IA 51041 -0487 |
| Contact | Donald F Riibe |
| Correspondent | Donald F Riibe MEDTEC, INC. P.O. BOX 487 1401 8TH STREET SOUTH EAST Orange City, IA 51041 -0487 |
| Product Code | IWE |
| CFR Regulation Number | 892.5780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-11-14 |
| Decision Date | 1996-05-24 |