The following data is part of a premarket notification filed by Meditron Corp. with the FDA for Telemedic Teleradiology System.
| Device ID | K921185 |
| 510k Number | K921185 |
| Device Name: | TELEMEDIC TELERADIOLOGY SYSTEM |
| Classification | System, Digital Image Communications, Radiological |
| Applicant | MEDITRON CORP. P.O. BOX 6419 Stateline, NV 89449 |
| Contact | Daniel P Aeberll |
| Correspondent | Daniel P Aeberll MEDITRON CORP. P.O. BOX 6419 Stateline, NV 89449 |
| Product Code | LMD |
| CFR Regulation Number | 892.2020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-03-09 |
| Decision Date | 1993-03-29 |