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FDA 510(k)

ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039

K-Number: K073441 · 2008-01-24

ApplicantPossis Medical, Inc.
Decision Date2008-01-24
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 is the device name listed in this FDA 510(k) record. The listed applicant is Possis Medical, Inc.. It received FDA 510(k) clearance on 2008-01-24 under 510(k) number K073441. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039?

ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 is a medical device that received FDA 510(k) clearance on 2008-01-24. The listed applicant is Possis Medical, Inc.. The 510(k) number is K073441.

When did ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 receive FDA 510(k) clearance?

ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 received FDA 510(k) clearance on 2008-01-24, under 510(k) number K073441.

Who is the listed applicant for ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039?

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

What is the FDA product code for ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039?

The FDA product code for ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 is QEZ.

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Other records listing Possis Medical, 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.

K091593ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETSK090253ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL 106552-001, ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040-001K082382ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039K081989MODIFICATION TO FETCH ASPIRATION CATHETERK081454GUARDDOG OCCLUSION GUIDEWIRE, INFLATION DEVICEK080806ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608

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Related Devices (Code: QEZ)

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.

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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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