MULTIGRAPH
FDA 510(k) clearance K790765 · decided 1979-04-26
Clearance details
- K-number
- K790765
- Device name
- MULTIGRAPH
- Applicant
- Siemens Corp.
- Decision
- Substantially Equivalent
- Date received
- 1979-04-19
- Decision date
- 1979-04-26
- Days to decision
- 7 days
- Clearance type
- Traditional
- Product code
- IZF
- Device class
- 2
- Regulation number
- 892.1740
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| 3D Ceiling Suspension recall (Z-0987-03) | Siemens Medical Solutions USA, Inc | 2003-07-10 |