Mtx Generator
by Philips Medical Systems (Cleveland), Inc.
510(k) K880352
Mtx Generator is a medical device (FDA Class II; FDA product code KPR, System, X-Ray, Stationary) made by Philips Medical Systems (Cleveland), Inc., cleared under FDA 510(k) K880352 on 14 Jul 1988, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK880352 | Date14 Jul 1988 | StatusActive |
Official records
- FDA 510(k) database K880352
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KPR
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1680
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code KPR (System, X-Ray, Stationary).
- DIAMOND-5A/6A/8A by DRGEM Corporation
- FUJI COMPUTED RADIOGRAPHY OD-F623 OPTICAL-DISK by Fujifilm Medical System U.S.A., Inc.
- Diamentor Patient X-Ray Exposure Indicator 07302 by Victoreen, Inc.
- Armboard by Mtd, Inc.
- Imasight 4600 Digital Radiography Sensor by Imasight, Inc.
- OTC DDR System by Konica Minolta Healthcare Americas, Inc
- Flaatz 760 by Drtech Corp.
- Z-Motion Digital Diagnostic X-Ray System by Control-X Medical, Inc.
- DR-ID 900MC DR-ID 900 MC E by FUJIFILM CORPORATION
- AeroDR System with P-21 by Konica Minolta Medical & Graphic, Inc.
Other devices from Philips Medical Systems (Cleveland), Inc.
See all devices from Philips Medical Systems (Cleveland), Inc. →