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FDA 510(k)

DE ORO 77

K-Number: K964476 · 1996-12-04

Decision Date1996-12-04
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DE ORO 77 is the device name listed in this FDA 510(k) record. The listed applicant is Gateway Alloys, Inc.. It received FDA 510(k) clearance on 1996-12-04 under 510(k) number K964476. 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 DE ORO 77?

DE ORO 77 is a medical device that received FDA 510(k) clearance on 1996-12-04. The listed applicant is Gateway Alloys, Inc.. The 510(k) number is K964476.

When did DE ORO 77 receive FDA 510(k) clearance?

DE ORO 77 received FDA 510(k) clearance on 1996-12-04, under 510(k) number K964476.

Who is the listed applicant for DE ORO 77?

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

What is the FDA product code for DE ORO 77?

The FDA product code for DE ORO 77 is EJT.

Other records listing Gateway Alloys, 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 31 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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