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FDA 510(k)

ACTION STORM RANGER II, ACTION STORM POWER 9000

K-Number: K982064 · 1998-10-05

Decision Date1998-10-05
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACTION STORM RANGER II, ACTION STORM POWER 9000 is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K982064. 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 ACTION STORM RANGER II, ACTION STORM POWER 9000?

ACTION STORM RANGER II, ACTION STORM POWER 9000 is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Invacare Corp.. The 510(k) number is K982064.

When did ACTION STORM RANGER II, ACTION STORM POWER 9000 receive FDA 510(k) clearance?

ACTION STORM RANGER II, ACTION STORM POWER 9000 received FDA 510(k) clearance on 1998-10-05, under 510(k) number K982064.

Who is the listed applicant for ACTION STORM RANGER II, ACTION STORM POWER 9000?

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 ACTION STORM RANGER II, ACTION STORM POWER 9000?

The FDA product code for ACTION STORM RANGER II, ACTION STORM POWER 9000 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 Invacare Corp. 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.

View all 111 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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