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)

LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001

K-Number: K031321 · 2004-01-21

ApplicantMedlogic Global Limited
Decision Date2004-01-21
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 is the device name listed in this FDA 510(k) record. The listed applicant is Medlogic Global Limited. It received FDA 510(k) clearance on 2004-01-21 under 510(k) number K031321. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001?

LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 is a medical device that received FDA 510(k) clearance on 2004-01-21. The listed applicant is Medlogic Global Limited. The 510(k) number is K031321.

When did LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 receive FDA 510(k) clearance?

LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 received FDA 510(k) clearance on 2004-01-21, under 510(k) number K031321.

Who is the listed applicant for LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001?

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

What is the FDA product code for LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001?

The FDA product code for LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 is KMF.

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 Medlogic Global Limited 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.

K110184LIQUIBAND FLOW CONTROLK102076LIQUIBAND DUAL, MODEL LBD 001K100284LIQUIBAND ULTIMA, LUT 003K023163LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020

Related Devices (Code: KMF)

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.

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLCK171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M HealthcareK160684Atteris No-Sting Skin ProtectantRochal Industries, LLCK120059LIQUID BANDAGEChesson Laboratory Associates, 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.

↑