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FDA 510(k)

MEDAMICUS FLOWGUARD PEELABLE INTRODUCER

K-Number: K030905 · 2003-04-09

Decision Date2003-04-09
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDAMICUS FLOWGUARD PEELABLE INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Medamicus, Inc.. It received FDA 510(k) clearance on 2003-04-09 under 510(k) number K030905. 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 MEDAMICUS FLOWGUARD PEELABLE INTRODUCER?

MEDAMICUS FLOWGUARD PEELABLE INTRODUCER is a medical device that received FDA 510(k) clearance on 2003-04-09. The listed applicant is Medamicus, Inc.. The 510(k) number is K030905.

When did MEDAMICUS FLOWGUARD PEELABLE INTRODUCER receive FDA 510(k) clearance?

MEDAMICUS FLOWGUARD PEELABLE INTRODUCER received FDA 510(k) clearance on 2003-04-09, under 510(k) number K030905.

Who is the listed applicant for MEDAMICUS FLOWGUARD PEELABLE INTRODUCER?

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

What is the FDA product code for MEDAMICUS FLOWGUARD PEELABLE INTRODUCER?

The FDA product code for MEDAMICUS FLOWGUARD PEELABLE INTRODUCER 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 Medamicus, 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.

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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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