BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE
K-Number: K111401 · 2012-07-19
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Device Summary
Frequently Asked Questions
What is the BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE?
BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 2012-07-19. The listed applicant is Hangzhou Bever Medical Devices Co., Ltd.. The 510(k) number is K111401.
When did BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE receive FDA 510(k) clearance?
BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE received FDA 510(k) clearance on 2012-07-19, under 510(k) number K111401.
Who is the listed applicant for BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE?
The FDA 510(k) record lists Hangzhou Bever Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE?
The FDA product code for BEVER ENDOTRACHEAL TUBE, BEVER EVA ENDOTRACHEAL TUBE is BTR.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Hangzhou Bever Medical Devices Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BTR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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