FDA 510(k) Applications Submitted by HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K111401 |
05/19/2011 |
BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE |
HANGZHOU BEVER MEDICAL DEVICES CO., LTD. |
K111405 |
05/19/2011 |
BEVER UNOCATED / COATED, PAEDIATRIC / MALE / FEMALE NELATON-TIP / TIEMANN-TIP INTERMITTENT CATHETER, |
HANGZHOU BEVER MEDICAL DEVICES CO., LTD. |
K111406 |
05/19/2011 |
BEVER REINFORCED ENDOTRACHEAL TUBE WITH CUFF (ORAL/NASAL), BEVER REINFORCED ENDOTRACHEAL TUBE WITHOUT CUFF (ORAL/NASAL) |
HANGZHOU BEVER MEDICAL DEVICES CO., LTD. |
K192468 |
09/09/2019 |
Male, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Femal, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Pediatric, Nelaton-tip Ready-to-Use Hydrophilic Catheter Intermittent Catheter; Male, Tapered-Tip Tiemann Ready-to-Use Hydrophilic Catheter; Male, O |
Hangzhou Bever Medical Devices Co., Ltd. |
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