Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Method Mobility. It received FDA 510(k) clearance on 2023-05-10 under 510(k) 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. The listed applicant is Method Mobility. The 510(k) number is K231032.

When did AMP by Method Mobility, AMP Plus (or +) by Method Mobility receive FDA 510(k) clearance?

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

Who is the listed applicant for AMP by Method Mobility, AMP Plus (or +) by Method Mobility?

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

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.

Related Devices (Code: ITI)

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.

K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.K261396Electric WheelchairNingbo Resshidi Medical Devices Co., Ltd.K261164Electric wheelchair (XW-LY007 )Yongkang Ruihe Metal Product Co., Ltd.K260937Smart Electric Wheelchair (R1-Std-BK, R1-Pro-BK, R1-Ultra-GK, R1-Ultra-WK)Shanghai Waylong Intelligent Technology Co.,LtdK253812Power Wheelchair (W5915B, W5915C, W5915D)Zhejiang Innuovo Rehabilitation Devices Co.,LtdK260335Electric Wheelchair (S500-6)Zhongshan Sulenz Intelligent Technology Co., Ltd.

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.

↑