510(k) · Cleared
ClearedAutomatic Exposure Control Type A3300
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Advanced Instrument Development, Inc.
Cleared on Jun 18, 1982 after a 28-day review. FDA has not posted a summary or statement for it, so its predicates are not known.
- Decided
- Jun 18, 1982
- Review
- 28 days
- Recalls
- None
- Predicates
- 0
FDA has not posted a summary or statement for it, so its predicates are not known.
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in this category? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
https://510kreport.com/device/K827525 · printed Nov 5, 2026
Cite this page
510(k) Report. “K827525: Automatic Exposure Control Type A3300.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K827525
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026