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FDA 510(k)

ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE

K-Number: K003415 · 2001-01-03

Decision Date2001-01-03
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Wang & Li, Inc.. It received FDA 510(k) clearance on 2001-01-03 under 510(k) number K003415. 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 WITH STETHOSCOPE?

ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2001-01-03. The listed applicant is Wang & Li, Inc.. The 510(k) number is K003415.

When did ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE receive FDA 510(k) clearance?

ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE received FDA 510(k) clearance on 2001-01-03, under 510(k) number K003415.

Who is the listed applicant for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE?

The FDA 510(k) record lists Wang & Li, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE?

The FDA product code for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE 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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