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FDA 510(k)

Al-Rad Companion (Musculoskeletal)

K-Number: K193267 · 2020-03-16

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-03-16
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Al-Rad Companion (Musculoskeletal) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2020-03-16 under approval number K193267. 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 Al-Rad Companion (Musculoskeletal)?

Al-Rad Companion (Musculoskeletal) is a medical device that received FDA 510(k) clearance on 2020-03-16. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K193267.

When was Al-Rad Companion (Musculoskeletal) approved by the FDA?

Al-Rad Companion (Musculoskeletal) received FDA 510(k) clearance on 2020-03-16, under approval number K193267.

What company makes Al-Rad Companion (Musculoskeletal)?

Al-Rad Companion (Musculoskeletal) is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for Al-Rad Companion (Musculoskeletal)?

The FDA product code for Al-Rad Companion (Musculoskeletal) is JAK.

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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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