MYDClass I

Keratome, Water Jet

21 CFR 886.4370 / Ophthalmic

MYD is the FDA product code for Keratome, Water Jet, a class I device type, regulated under 21 CFR 886.4370. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 2000-10-20, and no recalls.

Classification record

Product code: MYD
Device name: Keratome, Water Jet
Regulation: 21 CFR 886.4370
Device class: Class I
Review panel: Ophthalmic
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code MYD

By decision year

1 clearance under product code MYD with a decision year between 2000 and 2000, 2000 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code MYD by decision year
Year	Clearances
2000	1

Applicants with the most clearances

Product code MYD

Applicants holding the most 510(k) clearances under product code MYD
Applicant	Clearances
Visijet, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MYD.

Recent clearances

Product code MYD

K991124Class IVisijet Hydrokeratome, Model 50Visijet, Inc. / cleared 2000-10-20

Recent recalls

Product code MYD

FDA records show no recalls under product code MYD.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)