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FDA 510(k)

DIGITAL RADIOGRAPHY SYSTEM

K-Number: K827289 · 1982-04-21

ApplicantDiagnostic Technology, Inc.
Decision Date1982-04-21
Product Code
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Technology, Inc.. It received FDA 510(k) clearance on 1982-04-21 under 510(k) number K827289. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL RADIOGRAPHY SYSTEM?

DIGITAL RADIOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1982-04-21. The listed applicant is Diagnostic Technology, Inc.. The 510(k) number is K827289.

When did DIGITAL RADIOGRAPHY SYSTEM receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY SYSTEM received FDA 510(k) clearance on 1982-04-21, under 510(k) number K827289.

Who is the listed applicant for DIGITAL RADIOGRAPHY SYSTEM?

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

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Other records listing Diagnostic 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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