Product code HMS— Ophthalmic

MICRON-SCOPE II

Classification name: Drum, Eye Knife Test
Device class: Class 1
Regulation: 21 CFR 886.4230
Advisory panel: Ophthalmic
Total cleared: 1
First cleared: 1994-07-19
Most recent: 1994-07-19

Market context for product code HMS

FDA has cleared 1 device under product code HMS, all in 1994, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code HMS

Chiron Vision Corp.1 clearance

Recent clearances under product code HMS

K926412 — MICRON-SCOPE IIChiron Vision Corp.·1994-07-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.