The following data is part of a premarket notification filed by Medtec, Inc. with the FDA for Tungsten Eyeshield.
| Device ID | K943011 |
| 510k Number | K943011 |
| Device Name: | TUNGSTEN EYESHIELD |
| Classification | Shield, Eye, Radiological |
| Applicant | MEDTEC, INC. 1401 8TH ST. S.E. P.O. BOX 602 Orange City, IA 51041 |
| Contact | General Riibe |
| Correspondent | General Riibe MEDTEC, INC. 1401 8TH ST. S.E. P.O. BOX 602 Orange City, IA 51041 |
| Product Code | IWS |
| CFR Regulation Number | 892.6500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-06-24 |
| Decision Date | 1994-12-23 |