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FDA 510(k)

DGH-3000A A-SCAN

K-Number: K872726 · 1987-12-04

ApplicantDgh Technology, Inc.
Decision Date1987-12-04
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DGH-3000A A-SCAN is the device name listed in this FDA 510(k) record. The listed applicant is Dgh Technology, Inc.. It received FDA 510(k) clearance on 1987-12-04 under 510(k) number K872726. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DGH-3000A A-SCAN?

DGH-3000A A-SCAN is a medical device that received FDA 510(k) clearance on 1987-12-04. The listed applicant is Dgh Technology, Inc.. The 510(k) number is K872726.

When did DGH-3000A A-SCAN receive FDA 510(k) clearance?

DGH-3000A A-SCAN received FDA 510(k) clearance on 1987-12-04, under 510(k) number K872726.

Who is the listed applicant for DGH-3000A A-SCAN?

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

What is the FDA product code for DGH-3000A A-SCAN?

The FDA product code for DGH-3000A A-SCAN is IYO.

Other records listing Dgh Technology, 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.

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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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