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

Projector, Ophthalmic

21 CFR 886.1680 / Ophthalmic
FDA source (opens on fda.gov)

HOS is the FDA product code for Projector, Ophthalmic, a class I device type, regulated under 21 CFR 886.1680. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOS
Device name
Projector, Ophthalmic
Regulation
21 CFR 886.1680
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
9
Ingested recalls
0

Clearances, product code HOS

By decision year
9 clearances under product code HOS with a decision year between 1978 and 1994, 1981 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HOS by decision year
YearClearances
19781
19812
19861
19891
19921
19932
19941

Applicants with the most clearances

Product code HOS
Applicants holding the most 510(k) clearances under product code HOS
ApplicantClearances
Bausch & Lomb Incorporated2
American Optical Corp.1
Canon Medical Components U.S.A., Inc.1
Luneau Ophtalmologie SA1
Marco Ophthalmic, Inc.1
Mosebach Electric & Supply1
R.H. Burton Co.1
Woodlyn, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 37 companies shown, in name order