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FDA 510(k)

ADAC MODEL DPS-2800 DIGITAL PROCESSING SYSTEM

K-Number: K827581 · 1982-07-02

ApplicantAdac Laboratories
Decision Date1982-07-02
Product Code
DecisionSubstantially Equivalent

Device Summary

ADAC MODEL DPS-2800 DIGITAL PROCESSING 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 1982-07-02 under 510(k) number K827581. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAC MODEL DPS-2800 DIGITAL PROCESSING SYSTEM?

ADAC MODEL DPS-2800 DIGITAL PROCESSING SYSTEM is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Adac Laboratories. The 510(k) number is K827581.

When did ADAC MODEL DPS-2800 DIGITAL PROCESSING SYSTEM receive FDA 510(k) clearance?

ADAC MODEL DPS-2800 DIGITAL PROCESSING SYSTEM received FDA 510(k) clearance on 1982-07-02, under 510(k) number K827581.

Who is the listed applicant for ADAC MODEL DPS-2800 DIGITAL PROCESSING SYSTEM?

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

Related Clinical Trials

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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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

View all 88 devices →

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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