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FDA 510(k)

GDS-DCS

K-Number: K091367 · 2009-11-05

Decision Date2009-11-05
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GDS-DCS is the device name listed in this FDA 510(k) record. The listed applicant is Guided Delivery Systems. It received FDA 510(k) clearance on 2009-11-05 under 510(k) number K091367. 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 GDS-DCS?

GDS-DCS is a medical device that received FDA 510(k) clearance on 2009-11-05. The listed applicant is Guided Delivery Systems. The 510(k) number is K091367.

When did GDS-DCS receive FDA 510(k) clearance?

GDS-DCS received FDA 510(k) clearance on 2009-11-05, under 510(k) number K091367.

Who is the listed applicant for GDS-DCS?

The FDA 510(k) record lists Guided Delivery Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GDS-DCS?

The FDA product code for GDS-DCS is DYB.

Other records listing Guided Delivery Systems 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.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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