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
HOCClass I

Clip, Iris Retractor

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

HOC is the FDA product code for Clip, Iris Retractor, a class I device type, regulated under 21 CFR 886.4350. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HOC
Device name
Clip, Iris Retractor
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
2
Ingested recalls
0

Clearances, product code HOC

By decision year
2 clearances under product code HOC with a decision year between 1983 and 1987, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HOC by decision year
YearClearances
19831
19871

Applicants with the most clearances

Product code HOC
Applicants holding the most 510(k) clearances under product code HOC
ApplicantClearances
Medical Technical Products, Inc1
Phakosystems, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 58 companies shown, in name order