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FDA 510(k)

LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109

K-Number: K073260 · 2008-03-13

ApplicantDevice Partners International
Decision Date2008-03-13
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109 is the device name listed in this FDA 510(k) record. The listed applicant is Device Partners International. It received FDA 510(k) clearance on 2008-03-13 under 510(k) number K073260. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109?

LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109 is a medical device that received FDA 510(k) clearance on 2008-03-13. The listed applicant is Device Partners International. The 510(k) number is K073260.

When did LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109 receive FDA 510(k) clearance?

LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109 received FDA 510(k) clearance on 2008-03-13, under 510(k) number K073260.

Who is the listed applicant for LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109?

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

What is the FDA product code for LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109?

The FDA product code for LIISA LEVER INTEGRATED INTERVENTIONAL SYSTEM ADAPTER, MODEL VSL-109 is DTL.

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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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