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FDA 510(k)

SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES

K-Number: K052691 · 2006-05-17

Decision Date2006-05-17
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES is the device name listed in this FDA 510(k) record. The listed applicant is Suretek Medical. It received FDA 510(k) clearance on 2006-05-17 under 510(k) number K052691. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES?

SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES is a medical device that received FDA 510(k) clearance on 2006-05-17. The listed applicant is Suretek Medical. The 510(k) number is K052691.

When did SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES receive FDA 510(k) clearance?

SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES received FDA 510(k) clearance on 2006-05-17, under 510(k) number K052691.

Who is the listed applicant for SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES?

The FDA 510(k) record lists Suretek Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURETEK MEDICAL REPROCESSED COMPRESSION SLEEVES?

The FDA product code for SURETEK MEDICAL REPROCESSED 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 Suretek Medical 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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