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FDA 510(k)

DESERET EMBOLECTOMY/THROMBECTOMY CATH.

K-Number: K801650 · 1980-08-04

Decision Date1980-08-04
Product CodeDXE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DESERET EMBOLECTOMY/THROMBECTOMY CATH. is the device name listed in this FDA 510(k) record. The listed applicant is Deseret Medical, Inc.. It received FDA 510(k) clearance on 1980-08-04 under 510(k) number K801650. The device is classified under product code DXE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESERET EMBOLECTOMY/THROMBECTOMY CATH.?

DESERET EMBOLECTOMY/THROMBECTOMY CATH. is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Deseret Medical, Inc.. The 510(k) number is K801650.

When did DESERET EMBOLECTOMY/THROMBECTOMY CATH. receive FDA 510(k) clearance?

DESERET EMBOLECTOMY/THROMBECTOMY CATH. received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801650.

Who is the listed applicant for DESERET EMBOLECTOMY/THROMBECTOMY CATH.?

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

What is the FDA product code for DESERET EMBOLECTOMY/THROMBECTOMY CATH.?

The FDA product code for DESERET EMBOLECTOMY/THROMBECTOMY CATH. is DXE.

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 Deseret 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.

View all 20 devices →

Related Devices (Code: DXE)

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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