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FDA 510(k)

ACCUTRON POLLUTION REDUCER

K-Number: K790638 · 1979-05-25

Decision Date1979-05-25
Product CodeBSJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACCUTRON POLLUTION REDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1979-05-25 under 510(k) number K790638. The device is classified under product code BSJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTRON POLLUTION REDUCER?

ACCUTRON POLLUTION REDUCER is a medical device that received FDA 510(k) clearance on 1979-05-25. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K790638.

When did ACCUTRON POLLUTION REDUCER receive FDA 510(k) clearance?

ACCUTRON POLLUTION REDUCER received FDA 510(k) clearance on 1979-05-25, under 510(k) number K790638.

Who is the listed applicant for ACCUTRON POLLUTION REDUCER?

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

What is the FDA product code for ACCUTRON POLLUTION REDUCER?

The FDA product code for ACCUTRON POLLUTION REDUCER is BSJ.

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 Parker Laboratories, Inc. 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: BSJ)

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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