Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LOUSEBUSTER

K-Number: K093144 · 2009-12-16

ApplicantLarada Sciences
Decision Date2009-12-16
Product CodeLJL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LOUSEBUSTER is the device name listed in this FDA 510(k) record. The listed applicant is Larada Sciences. It received FDA 510(k) clearance on 2009-12-16 under 510(k) number K093144. 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 LOUSEBUSTER?

LOUSEBUSTER is a medical device that received FDA 510(k) clearance on 2009-12-16. The listed applicant is Larada Sciences. The 510(k) number is K093144.

When did LOUSEBUSTER receive FDA 510(k) clearance?

LOUSEBUSTER received FDA 510(k) clearance on 2009-12-16, under 510(k) number K093144.

Who is the listed applicant for LOUSEBUSTER?

The FDA 510(k) record lists Larada Sciences as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOUSEBUSTER?

The FDA product code for LOUSEBUSTER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Larada Sciences 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.

K083206LOUSEBUSTER

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.K083206LOUSEBUSTERLarada SciencesK991958KLOUT SHAMPOO AND LICE COMBING PRETREATMENT KITKiel Laboratories, Inc.K981147CLEAR (TM) LICE EGG REMOVER SYSTEMCare Technologies, Inc.K981250LICEMEISTER COMBNational Pediculosis Assoc.

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.

↑