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 760-N 4 WHEEL POWER WHEELCHAIR

K-Number: K921070 · 1992-05-26

Decision Date1992-05-26
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR 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 1992-05-26 under 510(k) number K921070. 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 FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR?

FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Fortress Scientific , Ltd.. The 510(k) number is K921070.

When did FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR receive FDA 510(k) clearance?

FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR received FDA 510(k) clearance on 1992-05-26, under 510(k) number K921070.

Who is the listed applicant for FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR?

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 760-N 4 WHEEL POWER WHEELCHAIR?

The FDA product code for FORTRESS 760-N 4 WHEEL POWER WHEELCHAIR is ITI.

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.

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.

View all 27 devices →

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.

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.

↑