The following data is part of a premarket notification filed by Konica Medical Corp. with the FDA for Konica Ld-4500 Laser Digitizer.
| Device ID | K933830 |
| 510k Number | K933830 |
| Device Name: | KONICA LD-4500 LASER DIGITIZER |
| Classification | Digitizer, Image, Radiological |
| Applicant | KONICA MEDICAL CORP. THE CHRYSLER BUILDING 405 LEXINGTON AVENUE New York, NY 10174 |
| Contact | Russell D Munves |
| Correspondent | Russell D Munves KONICA MEDICAL CORP. THE CHRYSLER BUILDING 405 LEXINGTON AVENUE New York, NY 10174 |
| Product Code | LMA |
| CFR Regulation Number | 892.2030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-08-05 |
| Decision Date | 1993-12-14 |