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FDA 510(k)

DPS-33,000 WITH CENTOR OPTION

K-Number: K881017 · 1988-08-11

ApplicantAdac Laboratories
Decision Date1988-08-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DPS-33,000 WITH CENTOR OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 1988-08-11 under 510(k) number K881017. 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 DPS-33,000 WITH CENTOR OPTION?

DPS-33,000 WITH CENTOR OPTION is a medical device that received FDA 510(k) clearance on 1988-08-11. The listed applicant is Adac Laboratories. The 510(k) number is K881017.

When did DPS-33,000 WITH CENTOR OPTION receive FDA 510(k) clearance?

DPS-33,000 WITH CENTOR OPTION received FDA 510(k) clearance on 1988-08-11, under 510(k) number K881017.

Who is the listed applicant for DPS-33,000 WITH CENTOR OPTION?

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 DPS-33,000 WITH CENTOR OPTION?

The FDA product code for DPS-33,000 WITH CENTOR OPTION is LLZ.

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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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Related Devices (Code: LLZ)

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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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