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FDA 510(k)

ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM

K-Number: K844298 · 1985-03-01

Decision Date1985-03-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADAC MODEL DPS-3300M 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 1985-03-01 under 510(k) number K844298. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM?

ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM is a medical device that received FDA 510(k) clearance on 1985-03-01. The listed applicant is Adac Laboratories. The 510(k) number is K844298.

When did ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM receive FDA 510(k) clearance?

ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM received FDA 510(k) clearance on 1985-03-01, under 510(k) number K844298.

Who is the listed applicant for ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM?

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

What is the FDA product code for ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM?

The FDA product code for ADAC MODEL DPS-3300M DIGITAL PROCESSING SYSTEM is LLZ.

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.

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.

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Related Devices (Code: LLZ)

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.

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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