Company ยท CN
Hangzhou Bever Medical Devices Co., Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2019. Name variants (Inc, Corp, punctuation) are merged.
4510(k) clearances (0 in 12 months)
1recalls (1 in 12 months)
1recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 27, 2019 | K192468 | Male, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Femal, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Pediatric, Ne Hangzhou Bever Medical Devices Co., Ltd., CN | GBM |
| Jul 19, 2012 | K111406 | BEVER REINFORCED ENDOTRACHEAL TUBE WITH CUFF (ORAL/NASAL), BEVER REINFORCED ENDOTRACHEAL TUBE WITHOUT CUFF (ORAL/NASAL) Hangzhou Bever Medical Devices Co., Ltd., CN | BTR |
| Jul 19, 2012 | K111401 | BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE Hangzhou Bever Medical Devices Co., Ltd., CN | BTR |
| Feb 13, 2012 | K111405 | BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER, Hangzhou Bever Medical Devices Co., Ltd., CN | GBM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 12, 2026 | HANGZHOU BEVER MEDICAL DEVICES CO., LTD. BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female
REF: RTU14F Open, Classified |
GBM | K192468 |