510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
HMDClass I

Chair, Ophthalmic, Manual

21 CFR 886.1140 / Ophthalmic
FDA source (opens on fda.gov)

HMD is the FDA product code for Chair, Ophthalmic, Manual, a class I device type, regulated under 21 CFR 886.1140. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
HMD
Device name
Chair, Ophthalmic, Manual
Regulation
21 CFR 886.1140
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code HMD

By decision year
1 clearance under product code HMD with a decision year between 1984 and 1984, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HMD by decision year
YearClearances
19841

Applicants with the most clearances

Product code HMD
Applicants holding the most 510(k) clearances under product code HMD
ApplicantClearances
Vision Health Technology1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 17 companies shown, in name order