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MICROVASIVE INSURG LAPTIE SUTURE LIGATOR

K931379 Class I Traditional
Decision Date
1993-07-13
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K931379
Product Code HCF
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1993-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROVASIVE INSURG LAPTIE SUTURE LIGATOR received FDA 510(k) clearance under submission number K931379, sponsored by Boston Scientific Corp. 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 1993-07-13.

Classification & Regulation

This clearance is catalogued under FDA product code HCF and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.