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TENSION-ISOMETER

K854254 Class I Traditional
Decision Date
1985-11-15
Sponsor / Applicant
Medmetric Corp.

Technical Specification

510(k) Submission ID K854254
Product Code LXI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1985-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TENSION-ISOMETER received FDA 510(k) clearance under submission number K854254, sponsored by Medmetric 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 1985-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code LXI and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.