UUHC REPROCESSED COMPRESSION SLEEVE DEVICES
K-Number: K031189 · 2003-10-16
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Device Summary
Frequently Asked Questions
What is the UUHC REPROCESSED COMPRESSION SLEEVE DEVICES?
UUHC REPROCESSED COMPRESSION SLEEVE DEVICES is a medical device that received FDA 510(k) clearance on 2003-10-16. The listed applicant is University of Utah Hospitals and Clinics. The 510(k) number is K031189.
When did UUHC REPROCESSED COMPRESSION SLEEVE DEVICES receive FDA 510(k) clearance?
UUHC REPROCESSED COMPRESSION SLEEVE DEVICES received FDA 510(k) clearance on 2003-10-16, under 510(k) number K031189.
Who is the listed applicant for UUHC REPROCESSED COMPRESSION SLEEVE DEVICES?
The FDA 510(k) record lists University of Utah Hospitals and Clinics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UUHC REPROCESSED COMPRESSION SLEEVE DEVICES?
The FDA product code for UUHC REPROCESSED COMPRESSION SLEEVE DEVICES 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 University of Utah Hospitals and Clinics 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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