The following data is part of a premarket notification filed by Newport Medical Instruments with the FDA for Newport C250 Air Compressor Model C250.
| Device ID | K041406 |
| 510k Number | K041406 |
| Device Name: | NEWPORT C250 AIR COMPRESSOR MODEL C250 |
| Classification | Compressor, Air, Portable |
| Applicant | NEWPORT MEDICAL INSTRUMENTS 760 W 16TH STREET, BLDG. N Costa Mesa, CA 92627 |
| Contact | Richard Waters |
| Correspondent | Richard Waters NEWPORT MEDICAL INSTRUMENTS 760 W 16TH STREET, BLDG. N Costa Mesa, CA 92627 |
| Product Code | BTI |
| CFR Regulation Number | 868.6250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-05-26 |
| Decision Date | 2004-12-15 |
| Summary: | summary |