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FDA 510(k)

MODEL PDX-4800 PROJECTION DIGITAL X-RAY SYSTEM

K-Number: K828606 · 1983-01-03

ApplicantAdac Laboratories
Decision Date1983-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL PDX-4800 PROJECTION DIGITAL X-RAY 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 1983-01-03 under 510(k) number K828606. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL PDX-4800 PROJECTION DIGITAL X-RAY SYSTEM?

MODEL PDX-4800 PROJECTION DIGITAL X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 1983-01-03. The listed applicant is Adac Laboratories. The 510(k) number is K828606.

When did MODEL PDX-4800 PROJECTION DIGITAL X-RAY SYSTEM receive FDA 510(k) clearance?

MODEL PDX-4800 PROJECTION DIGITAL X-RAY SYSTEM received FDA 510(k) clearance on 1983-01-03, under 510(k) number K828606.

Who is the listed applicant for MODEL PDX-4800 PROJECTION DIGITAL X-RAY SYSTEM?

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

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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