510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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HODClass I

Clamp, Eyelid, Ophthalmic

21 CFR 886.4350 / Ophthalmic
FDA source (opens on fda.gov)

HOD is the FDA product code for Clamp, Eyelid, Ophthalmic, a class I device type, regulated under 21 CFR 886.4350. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOD
Device name
Clamp, Eyelid, Ophthalmic
Regulation
21 CFR 886.4350
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code HOD

By decision year
3 clearances under product code HOD with a decision year between 1983 and 1993, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HOD by decision year
YearClearances
19831
19891
19931

Applicants with the most clearances

Product code HOD
Applicants holding the most 510(k) clearances under product code HOD
ApplicantClearances
Keeler Instruments, Inc.1
R.H. Burton Co.1
Richard R. Anthony, M.D.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 63 companies shown, in name order