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FDA 510(k)

TECHNO-SCOPE VISUAL STETHOSCOPE

K-Number: K050097 · 2005-09-30

Decision Date2005-09-30
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TECHNO-SCOPE VISUAL STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Techtrade, LLC. It received FDA 510(k) clearance on 2005-09-30 under 510(k) number K050097. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNO-SCOPE VISUAL STETHOSCOPE?

TECHNO-SCOPE VISUAL STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2005-09-30. The listed applicant is Techtrade, LLC. The 510(k) number is K050097.

When did TECHNO-SCOPE VISUAL STETHOSCOPE receive FDA 510(k) clearance?

TECHNO-SCOPE VISUAL STETHOSCOPE received FDA 510(k) clearance on 2005-09-30, under 510(k) number K050097.

Who is the listed applicant for TECHNO-SCOPE VISUAL STETHOSCOPE?

The FDA 510(k) record lists Techtrade, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECHNO-SCOPE VISUAL STETHOSCOPE?

The FDA product code for TECHNO-SCOPE VISUAL STETHOSCOPE is DQD.

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.

Other records listing Techtrade, LLC as applicant

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: DQD)

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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