ACTION STORM RANGER II, ACTION STORM POWER 9000
K-Number: K982064 · 1998-10-05
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Device Summary
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.
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
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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