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FDA 510(k)

GDC-591

K-Number: K790006 · 1979-02-27

Decision Date1979-02-27
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GDC-591 is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790006. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 46 devices →

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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