meddevicedb.com FDA Device Reference

#SM-3001 OPHTHA OTOSC SET SUBSETS SOLD

K852953 Class II Traditional
Decision Date
1985-09-06
Sponsor / Applicant
Design Med. Corp.

Technical Specification

510(k) Submission ID K852953
Product Code HLJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1570
Decision Date 1985-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

#SM-3001 OPHTHA OTOSC SET SUBSETS SOLD received FDA 510(k) clearance under submission number K852953, sponsored by Design Med. Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1985-09-06.

Classification & Regulation

This clearance is catalogued under FDA product code HLJ and 21 CFR 886.1570, within the Ophthalmic review panel as a Class II device.