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FDA 510(k)

A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH

K-Number: K092097 · 2010-05-06

Decision Date2010-05-06
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is A.B. Korkor Medical, Inc.. It received FDA 510(k) clearance on 2010-05-06 under 510(k) number K092097. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH?

A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH is a medical device that received FDA 510(k) clearance on 2010-05-06. The listed applicant is A.B. Korkor Medical, Inc.. The 510(k) number is K092097.

When did A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH receive FDA 510(k) clearance?

A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH received FDA 510(k) clearance on 2010-05-06, under 510(k) number K092097.

Who is the listed applicant for A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH?

The FDA 510(k) record lists A.B. Korkor Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH?

The FDA product code for A.B. KORKOR MEDICAL SKINNYSAFE INTRODUCER SHEATH is DYB.

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.

Related Devices (Code: DYB)

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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