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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 the device name listed in this FDA 510(k) record. The listed applicant is .Decimal, LLC. It received FDA 510(k) clearance on 2018-05-15 under 510(k) 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. The listed applicant is .Decimal, LLC. The 510(k) number is K173940.

When did Astroid Planning App receive FDA 510(k) clearance?

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

Who is the listed applicant for Astroid Planning App?

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

What is the FDA product code for Astroid Planning App?

The FDA product code for Astroid Planning App is MUJ.

Other records listing .Decimal, LLC as applicant

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.

K211511decimal BolusK192554decimal3D

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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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