The following data is part of a premarket notification filed by Analogic Corp. with the FDA for Digital Image Communications System.
| Device ID | K933103 |
| 510k Number | K933103 |
| Device Name: | DIGITAL IMAGE COMMUNICATIONS SYSTEM |
| Classification | System, Digital Image Communications, Radiological |
| Applicant | ANALOGIC CORP. 8 CENTENNIAL DR. Peabody, MA 01960 |
| Contact | Ronald Luich |
| Correspondent | Ronald Luich ANALOGIC CORP. 8 CENTENNIAL DR. Peabody, MA 01960 |
| Product Code | LMD |
| CFR Regulation Number | 892.2020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-24 |
| Decision Date | 1993-10-05 |