FORTRESS 760FS POWER WHEELCHAIR
K-Number: K900038 · 1990-01-12
Device Summary
Frequently Asked Questions
What is the FORTRESS 760FS POWER WHEELCHAIR?
FORTRESS 760FS POWER WHEELCHAIR 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 K900038.
When did FORTRESS 760FS POWER WHEELCHAIR receive FDA 510(k) clearance?
FORTRESS 760FS POWER WHEELCHAIR received FDA 510(k) clearance on 1990-01-12, under 510(k) number K900038.
Who is the listed applicant for FORTRESS 760FS 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 760FS POWER WHEELCHAIR?
The FDA product code for FORTRESS 760FS 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.
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.