The following data is part of a premarket notification filed by Philips Medical Systems(cleveland), Inc. with the FDA for Rapido 2000 Automatic Radiographic Table.
| Device ID | K943926 |
| 510k Number | K943926 |
| Device Name: | RAPIDO 2000 AUTOMATIC RADIOGRAPHIC TABLE |
| Classification | Table, Radiographic, Non-tilting, Powered |
| Applicant | PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. Cleveland, OH 44143 |
| Contact | Robert L Turocy |
| Correspondent | Robert L Turocy PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. 595 MINER RD. Cleveland, OH 44143 |
| Product Code | IZZ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-12 |
| Decision Date | 1994-11-28 |