TECHNO-SCOPE VISUAL STETHOSCOPE
K-Number: K050097 · 2005-09-30
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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