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FDA 510(k)

Astroid Planning App

K-Number: K173940 · 2018-05-15

Applicant.Decimal, LLC
Decision Date2018-05-15
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Astroid Planning App is a medical device manufactured by .Decimal, LLC. It received FDA 510(k) clearance on 2018-05-15 under approval number K173940. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Astroid Planning App?

Astroid Planning App is a medical device that received FDA 510(k) clearance on 2018-05-15. It is manufactured by .Decimal, LLC. The 510(k) number is K173940.

When was Astroid Planning App approved by the FDA?

Astroid Planning App received FDA 510(k) clearance on 2018-05-15, under approval number K173940.

What company makes Astroid Planning App?

Astroid Planning App is manufactured by .Decimal, LLC.

What is the FDA product code for Astroid Planning App?

The FDA product code for Astroid Planning App is MUJ.

Other Devices by .Decimal, LLC

K192554decimal3D K211511decimal Bolus

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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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