Kessel Medintim GmbH FDA Record
Kessel Medintim GmbH has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Kessel Medintim GmbH" is on file.
- Latest 510(k)
- Aug 26, 2014
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 1 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K140305 | CAYA CONTOURED DIAPHRAGM | Aug 26, 2014 |
Kessel Medintim GmbH and the FDA: common questions
Has Kessel Medintim GmbH received an FDA warning letter?
No FDA warning letter addressed to the name "Kessel Medintim GmbH" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Kessel Medintim GmbH received an FDA Form 483?
FDA has not published a Form 483 for "Kessel Medintim GmbH" in its reading room. FDA publishes some Form 483s, not all of them.
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