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FDA 510(k)

CLEAN SOURCE I, MODEL CS1000

K-Number: K981144 · 1998-09-15

ApplicantAquarius Technologies, Inc.
Decision Date1998-09-15
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEAN SOURCE I, MODEL CS1000 is the device name listed in this FDA 510(k) record. The listed applicant is Aquarius Technologies, Inc.. It received FDA 510(k) clearance on 1998-09-15 under 510(k) number K981144. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAN SOURCE I, MODEL CS1000?

CLEAN SOURCE I, MODEL CS1000 is a medical device that received FDA 510(k) clearance on 1998-09-15. The listed applicant is Aquarius Technologies, Inc.. The 510(k) number is K981144.

When did CLEAN SOURCE I, MODEL CS1000 receive FDA 510(k) clearance?

CLEAN SOURCE I, MODEL CS1000 received FDA 510(k) clearance on 1998-09-15, under 510(k) number K981144.

Who is the listed applicant for CLEAN SOURCE I, MODEL CS1000?

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

What is the FDA product code for CLEAN SOURCE I, MODEL CS1000?

The FDA product code for CLEAN SOURCE I, MODEL CS1000 is EIA.

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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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