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FDA 510(k)

ScannerSide DoseCheck

K-Number: K171261 · 2017-08-18

ApplicantRight Dose, Inc.
Decision Date2017-08-18
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ScannerSide DoseCheck is a medical device manufactured by Right Dose, Inc.. It received FDA 510(k) clearance on 2017-08-18 under approval number K171261. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ScannerSide DoseCheck?

ScannerSide DoseCheck is a medical device that received FDA 510(k) clearance on 2017-08-18. It is manufactured by Right Dose, Inc.. The 510(k) number is K171261.

When was ScannerSide DoseCheck approved by the FDA?

ScannerSide DoseCheck received FDA 510(k) clearance on 2017-08-18, under approval number K171261.

What company makes ScannerSide DoseCheck?

ScannerSide DoseCheck is manufactured by Right Dose, Inc..

What is the FDA product code for ScannerSide DoseCheck?

The FDA product code for ScannerSide DoseCheck is JAK.

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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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