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FDA 510(k)

LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020

K-Number: K023163 · 2003-01-13

ApplicantMedlogic Global Limited
Decision Date2003-01-13
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 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 2003-01-13 under 510(k) number K023163. 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-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020?

LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 is a medical device that received FDA 510(k) clearance on 2003-01-13. The listed applicant is Medlogic Global Limited. The 510(k) number is K023163.

When did LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 receive FDA 510(k) clearance?

LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 received FDA 510(k) clearance on 2003-01-13, under 510(k) number K023163.

Who is the listed applicant for LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020?

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-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020?

The FDA product code for LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 is KMF.

Related Clinical Trials

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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 003K031321LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001

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

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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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