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FDA 510(k)

PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90

K-Number: K092285 · 2009-08-28

ApplicantBest Medical Canada , Ltd.
Decision Date2009-08-28
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90 is the device name listed in this FDA 510(k) record. The listed applicant is Best Medical Canada , Ltd.. It received FDA 510(k) clearance on 2009-08-28 under 510(k) number K092285. 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 PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90?

PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90 is a medical device that received FDA 510(k) clearance on 2009-08-28. The listed applicant is Best Medical Canada , Ltd.. The 510(k) number is K092285.

When did PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90 receive FDA 510(k) clearance?

PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90 received FDA 510(k) clearance on 2009-08-28, under 510(k) number K092285.

Who is the listed applicant for PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90?

The FDA 510(k) record lists Best Medical Canada , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90?

The FDA product code for PORTABLE DOSIMETER DOSE VERIFICATION SYSTEM, MODEL TD-RD-90 is IYE.

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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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