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FDA 510(k)

FORTRESS 1700FS REAR WHEEL DRIVE SCOOTER

K-Number: K922967 · 1992-08-03

ApplicantFortress Scientific , Ltd.
Decision Date1992-08-03
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORTRESS 1700FS REAR 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 1992-08-03 under 510(k) number K922967. 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 1700FS REAR WHEEL DRIVE SCOOTER?

FORTRESS 1700FS REAR WHEEL DRIVE SCOOTER is a medical device that received FDA 510(k) clearance on 1992-08-03. The listed applicant is Fortress Scientific , Ltd.. The 510(k) number is K922967.

When did FORTRESS 1700FS REAR WHEEL DRIVE SCOOTER receive FDA 510(k) clearance?

FORTRESS 1700FS REAR WHEEL DRIVE SCOOTER received FDA 510(k) clearance on 1992-08-03, under 510(k) number K922967.

Who is the listed applicant for FORTRESS 1700FS REAR 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 1700FS REAR WHEEL DRIVE SCOOTER?

The FDA product code for FORTRESS 1700FS REAR WHEEL DRIVE 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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