GDS-DCS
K-Number: K091367 · 2009-11-05
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Device Summary
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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