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FDA 510(k)

THE WAND MICROACCESS SAFETY INTRODUCER

K-Number: K090372 · 2009-03-30

Decision Date2009-03-30
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE WAND MICROACCESS SAFETY INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Access Scientific, Inc.. It received FDA 510(k) clearance on 2009-03-30 under 510(k) number K090372. 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 THE WAND MICROACCESS SAFETY INTRODUCER?

THE WAND MICROACCESS SAFETY INTRODUCER is a medical device that received FDA 510(k) clearance on 2009-03-30. The listed applicant is Access Scientific, Inc.. The 510(k) number is K090372.

When did THE WAND MICROACCESS SAFETY INTRODUCER receive FDA 510(k) clearance?

THE WAND MICROACCESS SAFETY INTRODUCER received FDA 510(k) clearance on 2009-03-30, under 510(k) number K090372.

Who is the listed applicant for THE WAND MICROACCESS SAFETY INTRODUCER?

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

What is the FDA product code for THE WAND MICROACCESS SAFETY INTRODUCER?

The FDA product code for THE WAND MICROACCESS SAFETY 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 Access Scientific, 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 8 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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