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)

FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER

K-Number: K900042 · 1990-01-12

ApplicantFortress Scientific , Ltd.
Decision Date1990-01-12
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER is the device name listed in this FDA 510(k) record. The listed applicant is Fortress Scientific , Ltd.. It received FDA 510(k) clearance on 1990-01-12 under 510(k) number K900042. 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 FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER?

FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is Fortress Scientific , Ltd.. The 510(k) number is K900042.

When did FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER receive FDA 510(k) clearance?

FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER received FDA 510(k) clearance on 1990-01-12, under 510(k) number K900042.

Who is the listed applicant for FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER?

The FDA 510(k) record lists Fortress Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER?

The FDA product code for FORTRESS BUDDY FRONT WHEEL DRIVE SCOOTER 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 Fortress Scientific , Ltd. 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.

K933855S490 SEATING SYSTEMK933864720 POWER BASEK933860S480 SEATING SYSTEMK933858730 POWER BASEK932597FORTRESS C-300 MICROPROCESSOR CONTROLLERK933853A901 TILT IN SPACE

View all 27 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.

↑