HOW · Class I · 21 CFR 886.1200

FDA Product Code HOW: Drum, Opticokinetic

Leading manufacturers include Life-Tech Intl., Inc..

1

Total

1

Cleared

31d

Avg days

1982

Since

FDA 510(k) Cleared Drum, Opticokinetic Devices (Product Code HOW)

1 devices

1–1 of 1

Cleared Nov 01, 1982

MODEL 5400 OPTOKINETIC STIMULATOR

Life-Tech Intl., Inc.

Ophthalmic · 31d

About Product Code HOW - Regulatory Context

Related FDA 510(k) Regulatory Insights

Data Source

FDA 510(k) public files . 175,730 total devices indexed.

Latest clearance: Nov 01, 1982

Product Code Info

Code	HOW
Device class	Class I
CFR	21 CFR 886.1200
Panel	Ophthalmic

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