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FDA 510(k)

INNOCOMB LICE COMB

K-Number: K822421 · 1982-10-13

ApplicantInnovative Products, Inc.
Decision Date1982-10-13
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INNOCOMB LICE COMB is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Products, Inc.. It received FDA 510(k) clearance on 1982-10-13 under 510(k) number K822421. 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 INNOCOMB LICE COMB?

INNOCOMB LICE COMB is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Innovative Products, Inc.. The 510(k) number is K822421.

When did INNOCOMB LICE COMB receive FDA 510(k) clearance?

INNOCOMB LICE COMB received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822421.

Who is the listed applicant for INNOCOMB LICE COMB?

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

What is the FDA product code for INNOCOMB LICE COMB?

The FDA product code for INNOCOMB LICE COMB is LJL.

Related Clinical Trials

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Other records listing Innovative Products, 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.

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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.

K151562Resultz Lice & Egg Removal KitPiedmont Pharmaceuticals, LLCK163401Nix Ultra Lice Treatment KitMedtech Products, Inc.K093144LOUSEBUSTERLarada SciencesK083206LOUSEBUSTERLarada SciencesK991958KLOUT SHAMPOO AND LICE COMBING PRETREATMENT KITKiel Laboratories, Inc.K981147CLEAR (TM) LICE EGG REMOVER SYSTEMCare Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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