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RUBBER BAND, STERILE

K882695 Class I Traditional
Decision Date
1988-10-13
Sponsor / Applicant
Bioseal

Technical Specification

510(k) Submission ID K882695
Product Code ECI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5410
Decision Date 1988-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RUBBER BAND, STERILE received FDA 510(k) clearance under submission number K882695, sponsored by Bioseal. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1988-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code ECI and 21 CFR 872.5410, within the Dental review panel as a Class I device.