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)

AMIGO MODEL 590000

K-Number: K983987 · 1999-06-08

ApplicantAmigo Mobility Intl., Inc.
Decision Date1999-06-08
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AMIGO MODEL 590000 is the device name listed in this FDA 510(k) record. The listed applicant is Amigo Mobility Intl., Inc.. It received FDA 510(k) clearance on 1999-06-08 under 510(k) number K983987. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMIGO MODEL 590000?

AMIGO MODEL 590000 is a medical device that received FDA 510(k) clearance on 1999-06-08. The listed applicant is Amigo Mobility Intl., Inc.. The 510(k) number is K983987.

When did AMIGO MODEL 590000 receive FDA 510(k) clearance?

AMIGO MODEL 590000 received FDA 510(k) clearance on 1999-06-08, under 510(k) number K983987.

Who is the listed applicant for AMIGO MODEL 590000?

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

What is the FDA product code for AMIGO MODEL 590000?

The FDA product code for AMIGO MODEL 590000 is INI.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Amigo Mobility Intl., Inc. as applicant

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.

K101507AMIGO CLASSIC FDK092936AMIGO ESCORT 7.5, MODEL 760001 PHSK010503AMIGO WHEELCHAIRK992619AMIGO MODEL 680000 (AMIGO EXCITE F 350)K981121AMIGO RTK952112AMIGO GRAND TOUR

View all 8 devices →

Related Devices (Code: INI)

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.

K261078Electric Scooter (FNS01,FNS03)Anhui Jbh Medical Apparatus Co., Ltd.K261859Electric Scooter (FDB08, FDB08A, FDB12)Anhui JBH Medical Apparatus Co., Ltd.K260094Mobility Scooter (W3465, W3902 (S50 Carbon))Zhejiang Innuovo Rehabilitation Devices Co.,LtdK260176Mobility Scooter (W3483, W3483A)Zhejiang Innuovo Rehabilitation Devices Co.,LtdK261232IERO Mobility Scooter (IERO-01)Jochu Technology Co., Ltd.K261163Mobility Scooter (R200)Yongkang Ruihe Metal Product 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.

↑