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FDA 510(k)

AMP by Method Mobility, AMP Plus (or +) by Method Mobility

K-Number: K231032 · 2023-05-10

ApplicantMethod Mobility
Decision Date2023-05-10
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AMP by Method Mobility, AMP Plus (or +) by Method Mobility is a medical device manufactured by Method Mobility. It received FDA 510(k) clearance on 2023-05-10 under approval number K231032. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

AMP by Method Mobility, AMP Plus (or +) by Method Mobility is a medical device that received FDA 510(k) clearance on 2023-05-10. It is manufactured by Method Mobility. The 510(k) number is K231032.

When was AMP by Method Mobility, AMP Plus (or +) by Method Mobility approved by the FDA?

AMP by Method Mobility, AMP Plus (or +) by Method Mobility received FDA 510(k) clearance on 2023-05-10, under approval number K231032.

What company makes AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

AMP by Method Mobility, AMP Plus (or +) by Method Mobility is manufactured by Method Mobility.

What is the FDA product code for AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

The FDA product code for AMP by Method Mobility, AMP Plus (or +) by Method Mobility is ITI.

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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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