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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 the device name listed in this FDA 510(k) record. The listed applicant is Blue Belt Technologies, Inc.. It received FDA 510(k) clearance on 2022-03-11 under 510(k) 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. The listed applicant is Blue Belt Technologies, Inc.. The 510(k) number is K212040.

When did RI.HIP MODELER receive FDA 510(k) clearance?

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

Who is the listed applicant for RI.HIP MODELER?

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

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

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

Other records listing Blue Belt Technologies, Inc. as applicant

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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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