The following data is part of a premarket notification filed by Philips Medical Systems(cleveland), Inc. with the FDA for Jpacs.
| Device ID | K980918 |
| 510k Number | K980918 |
| Device Name: | JPACS |
| Classification | System, Digital Image Communications, Radiological |
| 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 | LMD |
| CFR Regulation Number | 892.2020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-03-11 |
| Decision Date | 1998-06-03 |
| Summary: | summary |