BRACE, TENNIS ELBOW
K-Number: K780053 · 1978-01-17
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Device Summary
Frequently Asked Questions
What is the BRACE, TENNIS ELBOW?
BRACE, TENNIS ELBOW is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K780053.
When did BRACE, TENNIS ELBOW receive FDA 510(k) clearance?
BRACE, TENNIS ELBOW received FDA 510(k) clearance on 1978-01-17, under 510(k) number K780053.
Who is the listed applicant for BRACE, TENNIS ELBOW?
The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRACE, TENNIS ELBOW?
The FDA product code for BRACE, TENNIS ELBOW is IQI.
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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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: IQI)
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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