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AESCULAP HISTOACRYL FLEXIBLE TOPICAL SKIN ADHESIVE

K121976 Class II Traditional
Decision Date
2013-05-17
Sponsor / Applicant
Aesculap, Inc.

Technical Specification

510(k) Submission ID K121976
Product Code MPN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4010
Decision Date 2013-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AESCULAP HISTOACRYL FLEXIBLE TOPICAL SKIN ADHESIVE received FDA 510(k) clearance under submission number K121976, sponsored by Aesculap, Inc.. 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 2013-05-17.

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.