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FDA 510(k)

THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM

K-Number: K930506 · 1994-08-29

ApplicantPinecliff Assoc.
Decision Date1994-08-29
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pinecliff Assoc.. It received FDA 510(k) clearance on 1994-08-29 under 510(k) number K930506. 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 THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM?

THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-08-29. The listed applicant is Pinecliff Assoc.. The 510(k) number is K930506.

When did THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM receive FDA 510(k) clearance?

THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM received FDA 510(k) clearance on 1994-08-29, under 510(k) number K930506.

Who is the listed applicant for THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM?

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

What is the FDA product code for THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM?

The FDA product code for THERPAC RADIOTHERAPY TREATMENT PLANNING SYSTEM is IYE.

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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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