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FDA 510(k)

FORTRESS LIBERATOR RWD SCOOTER

K-Number: K900041 · 1990-01-12

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

Device Summary

FORTRESS LIBERATOR RWD 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 K900041. 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 LIBERATOR RWD SCOOTER?

FORTRESS LIBERATOR RWD 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 K900041.

When did FORTRESS LIBERATOR RWD SCOOTER receive FDA 510(k) clearance?

FORTRESS LIBERATOR RWD SCOOTER received FDA 510(k) clearance on 1990-01-12, under 510(k) number K900041.

Who is the listed applicant for FORTRESS LIBERATOR RWD 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 LIBERATOR RWD SCOOTER?

The FDA product code for FORTRESS LIBERATOR RWD SCOOTER is INI.

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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.

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