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)

MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER

K-Number: K950778 · 1995-03-14

Decision Date1995-03-14
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Medifriend Medical Products Co., Ltd.. It received FDA 510(k) clearance on 1995-03-14 under 510(k) number K950778. 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 MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER?

MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1995-03-14. The listed applicant is Shanghai Medifriend Medical Products Co., Ltd.. The 510(k) number is K950778.

When did MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER receive FDA 510(k) clearance?

MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER received FDA 510(k) clearance on 1995-03-14, under 510(k) number K950778.

Who is the listed applicant for MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER?

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

What is the FDA product code for MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER?

The FDA product code for MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER 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.

↑