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FDA 510(k)

MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM

K-Number: K827502 · 1982-06-09

ApplicantAdac Laboratories
Decision Date1982-06-09
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1982-06-09 under 510(k) number K827502. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM?

MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1982-06-09. The listed applicant is Adac Laboratories. The 510(k) number is K827502.

When did MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM receive FDA 510(k) clearance?

MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM received FDA 510(k) clearance on 1982-06-09, under 510(k) number K827502.

Who is the listed applicant for MODEL DPS-4050 DIGITAL RADIOGRAPHY SYSTEM?

The FDA 510(k) record lists Adac Laboratories as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Adac Laboratories 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.

K062298APOLLO GAMMA CAMERA SYSTEMK061029JETSTREAM WORKSPACEK060020AUTOQUANT PLUSK051351PRECEDENCE SPECT/CT IMAGING SYSTEMK042880JETSTREAM WORKSPACEK042903AUTOSPECS

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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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