Automatic Exposure Control Type A3300
FDA 510(k) K827525 · Advanced Instrument Development, Inc.
510(k) numberK827525
Submission
- Device name
- Automatic Exposure Control Type A3300
- Applicant
- Advanced Instrument Development, Inc.
Melrose Park, IL, US - Received
- May 21, 1982
- Decision date
- June 18, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Advanced Instrument Development, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K974863 | Imix Digital Thorax SystemKPR · Traditional | 03/17/1998SE |
| K872445 | Power-Aid Independent X-Ray Power SourceIZO · Traditional | 08/12/1987SE |
| K813128 | Mobil-Aid Automatic Exposure ControlIZL · Traditional | 12/03/1981SE |
| K791933 | Conversion Contractor Timer KitIZO · Traditional | 11/13/1979SE |
Questions and answers
When was Automatic Exposure Control Type A3300 cleared by the FDA?
Automatic Exposure Control Type A3300 (K827525) received a 510(k) decision of Substantially Equivalent on June 18, 1982, 28 days after the submission was received.