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FDA 510(k)

CLEAR (TM) LICE EGG REMOVER SYSTEM

K-Number: K981147 · 1998-06-09

Decision Date1998-06-09
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLEAR (TM) LICE EGG REMOVER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Care Technologies, Inc.. It received FDA 510(k) clearance on 1998-06-09 under 510(k) number K981147. The device is classified under product code LJL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR (TM) LICE EGG REMOVER SYSTEM?

CLEAR (TM) LICE EGG REMOVER SYSTEM is a medical device that received FDA 510(k) clearance on 1998-06-09. The listed applicant is Care Technologies, Inc.. The 510(k) number is K981147.

When did CLEAR (TM) LICE EGG REMOVER SYSTEM receive FDA 510(k) clearance?

CLEAR (TM) LICE EGG REMOVER SYSTEM received FDA 510(k) clearance on 1998-06-09, under 510(k) number K981147.

Who is the listed applicant for CLEAR (TM) LICE EGG REMOVER SYSTEM?

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

What is the FDA product code for CLEAR (TM) LICE EGG REMOVER SYSTEM?

The FDA product code for CLEAR (TM) LICE EGG REMOVER SYSTEM is LJL.

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 Care Technologies, 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: LJL)

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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