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FDA 510(k)

CLEAN UP

K-Number: K922985 · 1993-05-27

ApplicantBio-Probe, Inc.
Decision Date1993-05-27
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CLEAN UP is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Probe, Inc.. It received FDA 510(k) clearance on 1993-05-27 under 510(k) number K922985. 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 UP?

CLEAN UP is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is Bio-Probe, Inc.. The 510(k) number is K922985.

When did CLEAN UP receive FDA 510(k) clearance?

CLEAN UP received FDA 510(k) clearance on 1993-05-27, under 510(k) number K922985.

Who is the listed applicant for CLEAN UP?

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

What is the FDA product code for CLEAN UP?

The FDA product code for CLEAN UP is EIA.

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Other records listing Bio-Probe, 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.

K941532BIOCALEX 6/9

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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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