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FDA 510(k)

MICROCRUISER PLUS INTRODUCER SET

K-Number: K011790 · 2001-09-05

Decision Date2001-09-05
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROCRUISER PLUS INTRODUCER SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 2001-09-05 under 510(k) number K011790. 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 MICROCRUISER PLUS INTRODUCER SET?

MICROCRUISER PLUS INTRODUCER SET is a medical device that received FDA 510(k) clearance on 2001-09-05. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K011790.

When did MICROCRUISER PLUS INTRODUCER SET receive FDA 510(k) clearance?

MICROCRUISER PLUS INTRODUCER SET received FDA 510(k) clearance on 2001-09-05, under 510(k) number K011790.

Who is the listed applicant for MICROCRUISER PLUS INTRODUCER SET?

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

What is the FDA product code for MICROCRUISER PLUS INTRODUCER SET?

The FDA product code for MICROCRUISER PLUS INTRODUCER SET 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 Medical Device Technologies, 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 46 devices →

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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