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FDA 510(k)

AS101, BLOOD PRESSURE CUFF

K-Number: K060871 · 2006-06-09

Decision Date2006-06-09
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AS101, BLOOD PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Wenzhou Longwan Medical Instrument Company. It received FDA 510(k) clearance on 2006-06-09 under 510(k) number K060871. 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 AS101, BLOOD PRESSURE CUFF?

AS101, BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2006-06-09. The listed applicant is Wenzhou Longwan Medical Instrument Company. The 510(k) number is K060871.

When did AS101, BLOOD PRESSURE CUFF receive FDA 510(k) clearance?

AS101, BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2006-06-09, under 510(k) number K060871.

Who is the listed applicant for AS101, BLOOD PRESSURE CUFF?

The FDA 510(k) record lists Wenzhou Longwan Medical Instrument Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AS101, BLOOD PRESSURE CUFF?

The FDA product code for AS101, BLOOD PRESSURE CUFF is DXQ.

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.

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.

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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