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FDA 510(k)

RI.HIP MODELER

K-Number: K212040 · 2022-03-11

ApplicantBlue Belt Technologies, Inc.
Decision Date2022-03-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RI.HIP MODELER is a medical device manufactured by Blue Belt Technologies, Inc.. It received FDA 510(k) clearance on 2022-03-11 under approval number K212040. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RI.HIP MODELER?

RI.HIP MODELER is a medical device that received FDA 510(k) clearance on 2022-03-11. It is manufactured by Blue Belt Technologies, Inc.. The 510(k) number is K212040.

When was RI.HIP MODELER approved by the FDA?

RI.HIP MODELER received FDA 510(k) clearance on 2022-03-11, under approval number K212040.

What company makes RI.HIP MODELER?

RI.HIP MODELER is manufactured by Blue Belt Technologies, Inc..

What is the FDA product code for RI.HIP MODELER?

The FDA product code for RI.HIP MODELER is LLZ.

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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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