GDC-591
K-Number: K790006 · 1979-02-27
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Device Summary
Frequently Asked Questions
What is the GDC-591?
GDC-591 is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K790006.
When did GDC-591 receive FDA 510(k) clearance?
GDC-591 received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790006.
Who is the listed applicant for GDC-591?
The FDA 510(k) record lists Deringer-Ney, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GDC-591?
The FDA product code for GDC-591 is EJT.
Other records listing Deringer-Ney, 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.
Related Devices (Code: EJT)
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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