Tomographic System, Computerized
by Philips Medical Systems (Cleveland), Inc.
510(k) K772123
Tomographic System, Computerized is a Class II device made by Philips Medical Systems (Cleveland), Inc., cleared under FDA 510(k) K772123 on 21 Nov 1977, 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 | NumberK772123 | Date21 Nov 1977 | StatusActive |
Official records
- FDA 510(k) database K772123
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAK
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1750
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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