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FDA 510(k)

ROBI COMBI

K-Number: K930859 · 1994-02-28

ApplicantEpilady 2000, LLC
Decision Date1994-02-28
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ROBI COMBI is the device name listed in this FDA 510(k) record. The listed applicant is Epilady 2000, LLC. It received FDA 510(k) clearance on 1994-02-28 under 510(k) number K930859. 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 ROBI COMBI?

ROBI COMBI is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Epilady 2000, LLC. The 510(k) number is K930859.

When did ROBI COMBI receive FDA 510(k) clearance?

ROBI COMBI received FDA 510(k) clearance on 1994-02-28, under 510(k) number K930859.

Who is the listed applicant for ROBI COMBI?

The FDA 510(k) record lists Epilady 2000, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROBI COMBI?

The FDA product code for ROBI COMBI is LJL.

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Other records listing Epilady 2000, LLC 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.

K233224Epilaser ProK213105Epilaser AbsoluteK170970Epilaser

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

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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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