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FDA 510(k)

ANEROID SPHYGMOMANOMETER, MODEL BK2002

K-Number: K043286 · 2005-01-13

ApplicantWenzhou Bokang Instrument Co.,Ltd
Decision Date2005-01-13
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYGMOMANOMETER, MODEL BK2002 is the device name listed in this FDA 510(k) record. The listed applicant is Wenzhou Bokang Instrument Co.,Ltd. It received FDA 510(k) clearance on 2005-01-13 under 510(k) number K043286. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEROID SPHYGMOMANOMETER, MODEL BK2002?

ANEROID SPHYGMOMANOMETER, MODEL BK2002 is a medical device that received FDA 510(k) clearance on 2005-01-13. The listed applicant is Wenzhou Bokang Instrument Co.,Ltd. The 510(k) number is K043286.

When did ANEROID SPHYGMOMANOMETER, MODEL BK2002 receive FDA 510(k) clearance?

ANEROID SPHYGMOMANOMETER, MODEL BK2002 received FDA 510(k) clearance on 2005-01-13, under 510(k) number K043286.

Who is the listed applicant for ANEROID SPHYGMOMANOMETER, MODEL BK2002?

The FDA 510(k) record lists Wenzhou Bokang Instrument Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANEROID SPHYGMOMANOMETER, MODEL BK2002?

The FDA product code for ANEROID SPHYGMOMANOMETER, MODEL BK2002 is DXQ.

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Related Devices (Code: DXQ)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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