The following data is part of a premarket notification filed by Del Medical Systems Corp. with the FDA for Nd Vision-220 Adaptive Image Processessor.
| Device ID | K960301 |
| 510k Number | K960301 |
| Device Name: | ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | DEL MEDICAL SYSTEMS CORP. ONE COMMERCE PARK Valhalla, NY 10595 |
| Contact | Karl Weydig |
| Correspondent | Karl Weydig DEL MEDICAL SYSTEMS CORP. ONE COMMERCE PARK Valhalla, NY 10595 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-22 |
| Decision Date | 1996-09-30 |
| Summary: | summary |