FDA 510(k)

Sample Preservative Fluid

Numéro K : K222771 · 2024-06-26

DemandeurHangzhou Bioer Technology Co., Ltd.

Date de décision2024-06-26

Code produitQBD

Comité consultatifMI

DécisionSubstantially Equivalent

Résumé du dispositif

Sample Preservative Fluid is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Bioer Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-26 under 510(k) number K222771. The device is classified under product code QBD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Sample Preservative Fluid?

Sample Preservative Fluid is a medical device that received FDA 510(k) clearance on 2024-06-26. The listed applicant is Hangzhou Bioer Technology Co., Ltd.. The 510(k) number is K222771.

When did Sample Preservative Fluid receive FDA 510(k) clearance?

Sample Preservative Fluid received FDA 510(k) clearance on 2024-06-26, under 510(k) number K222771.

Who is the listed applicant for Sample Preservative Fluid?

The FDA 510(k) record lists Hangzhou Bioer Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sample Preservative Fluid?

The FDA product code for Sample Preservative Fluid is QBD.

Essais cliniques associés

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Dispositifs connexes (Code : QBD)

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Source officielle

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