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
HQWClass II

Clip, Tantalum, Ophthalmic

21 CFR 886.3100 / Ophthalmic
FDA source (opens on fda.gov)

HQW is the FDA product code for Clip, Tantalum, Ophthalmic, a class II device type, regulated under 21 CFR 886.3100. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HQW
Device name
Clip, Tantalum, Ophthalmic
Regulation
21 CFR 886.3100
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code HQW

By decision year
3 clearances under product code HQW with a decision year between 1984 and 1990, 1990 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HQW by decision year
YearClearances
19841
19902

Applicants with the most clearances

Product code HQW
Applicants holding the most 510(k) clearances under product code HQW
ApplicantClearances
Alcon Surgical, Inc.1
Grieshaber & Co.1
Storz Instrument Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code