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FDA 510(k)

VALVED TEARAWAY INTRODUCER GENERATION II

K-Number: K132498 · 2013-11-25

Decision Date2013-11-25
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VALVED TEARAWAY INTRODUCER GENERATION II is the device name listed in this FDA 510(k) record. The listed applicant is Medcomp (Medical Components, Inc.). It received FDA 510(k) clearance on 2013-11-25 under 510(k) number K132498. 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 VALVED TEARAWAY INTRODUCER GENERATION II?

VALVED TEARAWAY INTRODUCER GENERATION II is a medical device that received FDA 510(k) clearance on 2013-11-25. The listed applicant is Medcomp (Medical Components, Inc.). The 510(k) number is K132498.

When did VALVED TEARAWAY INTRODUCER GENERATION II receive FDA 510(k) clearance?

VALVED TEARAWAY INTRODUCER GENERATION II received FDA 510(k) clearance on 2013-11-25, under 510(k) number K132498.

Who is the listed applicant for VALVED TEARAWAY INTRODUCER GENERATION II?

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

What is the FDA product code for VALVED TEARAWAY INTRODUCER GENERATION II?

The FDA product code for VALVED TEARAWAY INTRODUCER GENERATION II 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.

Other records listing Medcomp (Medical Components, Inc.) 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: 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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