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FDA 510(k)

PC-PLAN

K-Number: K862065 · 1986-08-26

ApplicantDosimetrix, Inc.
Decision Date1986-08-26
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PC-PLAN is the device name listed in this FDA 510(k) record. The listed applicant is Dosimetrix, Inc.. It received FDA 510(k) clearance on 1986-08-26 under 510(k) number K862065. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PC-PLAN?

PC-PLAN is a medical device that received FDA 510(k) clearance on 1986-08-26. The listed applicant is Dosimetrix, Inc.. The 510(k) number is K862065.

When did PC-PLAN receive FDA 510(k) clearance?

PC-PLAN received FDA 510(k) clearance on 1986-08-26, under 510(k) number K862065.

Who is the listed applicant for PC-PLAN?

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

What is the FDA product code for PC-PLAN?

The FDA product code for PC-PLAN is IYE.

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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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