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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 the device name listed in this FDA 510(k) record. The listed applicant is Right Dose, Inc.. It received FDA 510(k) clearance on 2017-08-18 under 510(k) 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. The listed applicant is Right Dose, Inc.. The 510(k) number is K171261.

When did ScannerSide DoseCheck receive FDA 510(k) clearance?

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

Who is the listed applicant for ScannerSide DoseCheck?

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

What is the FDA product code for ScannerSide DoseCheck?

The FDA product code for ScannerSide DoseCheck is JAK.

Related Devices (Code: JAK)

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

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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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