T.E.D. SEQUENTIAL COMPRESSION SLEEVES
K-Number: K781357 · 1978-09-20
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Device Summary
Frequently Asked Questions
What is the T.E.D. SEQUENTIAL COMPRESSION SLEEVES?
T.E.D. SEQUENTIAL COMPRESSION SLEEVES is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Kendall Research Center. The 510(k) number is K781357.
When did T.E.D. SEQUENTIAL COMPRESSION SLEEVES receive FDA 510(k) clearance?
T.E.D. SEQUENTIAL COMPRESSION SLEEVES received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781357.
Who is the listed applicant for T.E.D. SEQUENTIAL COMPRESSION SLEEVES?
The FDA 510(k) record lists Kendall Research Center as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T.E.D. SEQUENTIAL COMPRESSION SLEEVES?
The FDA product code for T.E.D. SEQUENTIAL COMPRESSION SLEEVES is JOW.
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 Kendall Research Center 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: JOW)
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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