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FDA 510(k)

AQUACISER IN-POOL TREADMILL

K-Number: K925807 · 1993-03-24

Decision Date1993-03-24
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AQUACISER IN-POOL TREADMILL is the device name listed in this FDA 510(k) record. The listed applicant is Aquaciser, Inc.. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K925807. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUACISER IN-POOL TREADMILL?

AQUACISER IN-POOL TREADMILL is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Aquaciser, Inc.. The 510(k) number is K925807.

When did AQUACISER IN-POOL TREADMILL receive FDA 510(k) clearance?

AQUACISER IN-POOL TREADMILL received FDA 510(k) clearance on 1993-03-24, under 510(k) number K925807.

Who is the listed applicant for AQUACISER IN-POOL TREADMILL?

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

What is the FDA product code for AQUACISER IN-POOL TREADMILL?

The FDA product code for AQUACISER IN-POOL TREADMILL is BXB.

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 Aquaciser, Inc. 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: BXB)

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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