White River Concepts FDA Record
White River Concepts has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "White River Concepts" is on file.
- Latest 510(k)
- Nov 4, 1997
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 3 | 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 |
|---|---|---|
| K970488 | HYDROCHECK MICRO FILTER | Nov 4, 1997 |
| K964679 | WHITE RIVER AUTOMATIC BREAST PUMP | Jun 10, 1997 |
| K971231 | WHITE RIVER MINI MANUAL BREAST PUMP | May 19, 1997 |
White River Concepts and the FDA: common questions
Has White River Concepts received an FDA warning letter?
No FDA warning letter addressed to the name "White River Concepts" 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 White River Concepts received an FDA Form 483?
FDA has not published a Form 483 for "White River Concepts" in its reading room. FDA publishes some Form 483s, not all of them.
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