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)

MINUET LCD, MINUET LCD eco

K-Number: K180075 · 2018-08-06

ApplicantUnimom.Co
Decision Date2018-08-06
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MINUET LCD, MINUET LCD eco is the device name listed in this FDA 510(k) record. The listed applicant is Unimom.Co. It received FDA 510(k) clearance on 2018-08-06 under 510(k) number K180075. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINUET LCD, MINUET LCD eco?

MINUET LCD, MINUET LCD eco is a medical device that received FDA 510(k) clearance on 2018-08-06. The listed applicant is Unimom.Co. The 510(k) number is K180075.

When did MINUET LCD, MINUET LCD eco receive FDA 510(k) clearance?

MINUET LCD, MINUET LCD eco received FDA 510(k) clearance on 2018-08-06, under 510(k) number K180075.

Who is the listed applicant for MINUET LCD, MINUET LCD eco?

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

What is the FDA product code for MINUET LCD, MINUET LCD eco?

The FDA product code for MINUET LCD, MINUET LCD eco is HGX.

Other records listing Unimom.Co 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: HGX)

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.