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FDA 510(k)

P3IMRT TM

K-Number: K002237 · 2001-02-02

ApplicantAdac Laboratories
Decision Date2001-02-02
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

P3IMRT TM is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 2001-02-02 under 510(k) number K002237. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P3IMRT TM?

P3IMRT TM is a medical device that received FDA 510(k) clearance on 2001-02-02. The listed applicant is Adac Laboratories. The 510(k) number is K002237.

When did P3IMRT TM receive FDA 510(k) clearance?

P3IMRT TM received FDA 510(k) clearance on 2001-02-02, under 510(k) number K002237.

Who is the listed applicant for P3IMRT TM?

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 P3IMRT TM?

The FDA product code for P3IMRT TM is MUJ.

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: MUJ)

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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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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