meddevicedb.com FDA Device Reference

Meriglu Topical Skin Adhesive

K230981 Class II Traditional
Decision Date
2024-03-16
Sponsor / Applicant
M/s. Meril Endo Surgery Private Limited.

Technical Specification

510(k) Submission ID K230981
Product Code MPN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4010
Decision Date 2024-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Meriglu Topical Skin Adhesive received FDA 510(k) clearance under submission number K230981, sponsored by M/s. Meril Endo Surgery Private Limited.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code MPN and 21 CFR 878.4010, within the General, Plastic Surgery review panel as a Class II device.