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FDA 510(k)

CPS AIM SL SLITTABLE INNER CATHETER

K-Number: K082932 · 2008-12-12

Decision Date2008-12-12
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPS AIM SL SLITTABLE INNER CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is St Jude Medical. It received FDA 510(k) clearance on 2008-12-12 under 510(k) number K082932. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPS AIM SL SLITTABLE INNER CATHETER?

CPS AIM SL SLITTABLE INNER CATHETER is a medical device that received FDA 510(k) clearance on 2008-12-12. The listed applicant is St Jude Medical. The 510(k) number is K082932.

When did CPS AIM SL SLITTABLE INNER CATHETER receive FDA 510(k) clearance?

CPS AIM SL SLITTABLE INNER CATHETER received FDA 510(k) clearance on 2008-12-12, under 510(k) number K082932.

Who is the listed applicant for CPS AIM SL SLITTABLE INNER CATHETER?

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

What is the FDA product code for CPS AIM SL SLITTABLE INNER CATHETER?

The FDA product code for CPS AIM SL SLITTABLE INNER CATHETER is DQY.

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 St Jude 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.

View all 95 devices →

Related Devices (Code: DQY)

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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