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FDA 510(k)

STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL

K-Number: K993413 · 1999-12-15

ApplicantInvacare Corp.
Decision Date1999-12-15
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1999-12-15 under 510(k) number K993413. 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 STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL?

STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL is a medical device that received FDA 510(k) clearance on 1999-12-15. The listed applicant is Invacare Corp.. The 510(k) number is K993413.

When did STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL receive FDA 510(k) clearance?

STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL received FDA 510(k) clearance on 1999-12-15, under 510(k) number K993413.

Who is the listed applicant for STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL?

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 STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL?

The FDA product code for STORM SERIES, POWER 9000 SERIES AND POWER TIGER WITH GYROSCOPE CONTROL is ITI.

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Related Devices (Code: ITI)

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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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