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)

LIQUIBAND DENTAL

K-Number: K993556 · 2000-01-03

Decision Date2000-01-03
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIQUIBAND DENTAL is the device name listed in this FDA 510(k) record. The listed applicant is Medlogic Global Corp.. It received FDA 510(k) clearance on 2000-01-03 under 510(k) number K993556. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUIBAND DENTAL?

LIQUIBAND DENTAL is a medical device that received FDA 510(k) clearance on 2000-01-03. The listed applicant is Medlogic Global Corp.. The 510(k) number is K993556.

When did LIQUIBAND DENTAL receive FDA 510(k) clearance?

LIQUIBAND DENTAL received FDA 510(k) clearance on 2000-01-03, under 510(k) number K993556.

Who is the listed applicant for LIQUIBAND DENTAL?

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

What is the FDA product code for LIQUIBAND DENTAL?

The FDA product code for LIQUIBAND DENTAL is EMA.

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.

Other records listing Medlogic Global Corp. 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.

Related Devices (Code: EMA)

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.

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.

↑