meddevicedb.com FDA Device Reference

BIO-RAD MODULAR AIR COMPRESSOR

K895575 Class II Traditional
Decision Date
1989-10-31
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K895575
Product Code HKX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1930
Decision Date 1989-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-RAD MODULAR AIR COMPRESSOR received FDA 510(k) clearance under submission number K895575, sponsored by Bio-Rad. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1989-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code HKX and 21 CFR 886.1930, within the Ophthalmic review panel as a Class II device.