Philips Electronics UK Limited FDA Record
Philips Electronics UK Limited has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Philips Electronics UK Limited" is on file.
- Latest 510(k)
- Nov 5, 2010
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 |
|---|---|---|
| K101538 | HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP) | Nov 5, 2010 |
| K100495 | PHILIPS AVENT DIGITAL THERMOMETER SET, MODEL SCH540 | Jun 22, 2010 |
| K090167 | PHILIPS AVENT CLASSIC STAGE 2 AND 3 TEETHER, MODEL SCF882/01, SCF884/01, PHILIPS AVENT ANIMAL STAGE… | Jun 18, 2009 |
Philips Electronics UK Limited and the FDA: common questions
Has Philips Electronics UK Limited received an FDA warning letter?
No FDA warning letter addressed to the name "Philips Electronics UK Limited" 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 Philips Electronics UK Limited received an FDA Form 483?
FDA has not published a Form 483 for "Philips Electronics UK Limited" in its reading room. FDA publishes some Form 483s, not all of them.
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