KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE
K-Number: K932835 · 1993-08-06
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Device Summary
Frequently Asked Questions
What is the KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE?
KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K932835.
When did KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE receive FDA 510(k) clearance?
KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE received FDA 510(k) clearance on 1993-08-06, under 510(k) number K932835.
Who is the listed applicant for KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE?
The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE?
The FDA product code for KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE 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 Healthcare Products Co. Div.Of Tyco Health 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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