Product code HMM— Ophthalmic

DISTOMETER

Classification name: Distometer
Device class: Class 1
Regulation: 21 CFR 886.1190
Advisory panel: Ophthalmic
Total cleared: 2
First cleared: 1987-09-21
Most recent: 1988-07-01

Market context for product code HMM

FDA has cleared 2 devices under product code HMM between 1987 and 1988, filed by 2 applicant companies. 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.

Clearances per year

19881 clearance
19871 clearance

Top applicants under product code HMM

Hagg-Streit Service, Inc.1 clearance
Allegheny Plastics, Inc.1 clearance

Recent clearances under product code HMM

K882575 — DISTOMETERHagg-Streit Service, Inc.·1988-07-01
K873440 — RULE, PUPILLARYAllegheny Plastics, Inc.·1987-09-21

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