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FDA 510(k)

TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER

K-Number: K901586 · 1990-04-16

ApplicantInvacare Corp.
Decision Date1990-04-16
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K901586. 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 TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER?

TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Invacare Corp.. The 510(k) number is K901586.

When did TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER receive FDA 510(k) clearance?

TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER received FDA 510(k) clearance on 1990-04-16, under 510(k) number K901586.

Who is the listed applicant for TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER?

The FDA product code for TRI-ROLLS REAR WHEEL DRIVE POWERED SCOOTER is INI.

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Related Devices (Code: 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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