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FDA 510(k)

THE ADVENTURER

K-Number: K881410 · 1988-04-21

ApplicantWestport Mobility Products, Inc.
Decision Date1988-04-21
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE ADVENTURER is the device name listed in this FDA 510(k) record. The listed applicant is Westport Mobility Products, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881410. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ADVENTURER?

THE ADVENTURER is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Westport Mobility Products, Inc.. The 510(k) number is K881410.

When did THE ADVENTURER receive FDA 510(k) clearance?

THE ADVENTURER received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881410.

Who is the listed applicant for THE ADVENTURER?

The FDA 510(k) record lists Westport Mobility Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE ADVENTURER?

The FDA product code for THE ADVENTURER is IOR.

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Related Devices (Code: IOR)

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.

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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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