Shenzhen Vistar Medical Supplies Co., Ltd. FDA Record
- No warning letters matched by name
Shenzhen Vistar Medical Supplies Co., Ltd. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Shenzhen Vistar Medical Supplies Co., Ltd." is on file.
- Latest 510(k)
- Oct 29, 2015
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 2 | 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 |
|---|---|---|
| K152465 | Disposable Blood Pressure Cuff | Oct 29, 2015 |
| K152468 | Reusable Blood Pressure Cuff | Oct 29, 2015 |
Shenzhen Vistar Medical Supplies Co., Ltd. and the FDA: common questions
Has Shenzhen Vistar Medical Supplies Co., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Shenzhen Vistar Medical Supplies Co., Ltd." 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 Shenzhen Vistar Medical Supplies Co., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Shenzhen Vistar Medical Supplies Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
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