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FDA 510(k)

AQUACISER II

K-Number: K925193 · 1994-08-26

ApplicantAquaciser, Inc.
Decision Date1994-08-26
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AQUACISER II is the device name listed in this FDA 510(k) record. The listed applicant is Aquaciser, Inc.. It received FDA 510(k) clearance on 1994-08-26 under 510(k) number K925193. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUACISER II?

AQUACISER II is a medical device that received FDA 510(k) clearance on 1994-08-26. The listed applicant is Aquaciser, Inc.. The 510(k) number is K925193.

When did AQUACISER II receive FDA 510(k) clearance?

AQUACISER II received FDA 510(k) clearance on 1994-08-26, under 510(k) number K925193.

Who is the listed applicant for AQUACISER II?

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 II?

The FDA product code for AQUACISER II is ILJ.

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.

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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.

K925807AQUACISER IN-POOL TREADMILLK890548AQUACISER SYSTEM

Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.

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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