meddevicedb.com FDA Device Reference

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS

K851792 Class I Traditional
Decision Date
1985-05-30
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851792
Product Code HNR
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4350
Decision Date 1985-05-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

37-940 TO 37-944 VARIOUS NOYES OPHTHALMIC FORCEPS received FDA 510(k) clearance under submission number K851792, sponsored by Artiberia. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-05-30.

Classification & Regulation

This clearance is catalogued under FDA product code HNR and 21 CFR 886.4350, within the Ophthalmic review panel as a Class I device.