Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A

K-Number: K051021 · 2005-06-20

Decision Date2005-06-20
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Lord International Trade Co., Ltd.. It received FDA 510(k) clearance on 2005-06-20 under 510(k) number K051021. 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 SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A?

ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A is a medical device that received FDA 510(k) clearance on 2005-06-20. The listed applicant is Shanghai Lord International Trade Co., Ltd.. The 510(k) number is K051021.

When did ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A receive FDA 510(k) clearance?

ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A received FDA 510(k) clearance on 2005-06-20, under 510(k) number K051021.

Who is the listed applicant for ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A?

The FDA 510(k) record lists Shanghai Lord International Trade Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A?

The FDA product code for ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A 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

View on FDA Database →

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

↑