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

Implant, Absorbable, (Scleral Buckling Methods)

21 CFR 886.3300 / Ophthalmic
FDA source (opens on fda.gov)

HQJ is the FDA product code for Implant, Absorbable, (Scleral Buckling Methods), a class II device type, regulated under 21 CFR 886.3300. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
HQJ
Device name
Implant, Absorbable, (Scleral Buckling Methods)
Regulation
21 CFR 886.3300
Device class
Class II
Review panel
Ophthalmic
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code HQJ

By decision year
5 clearances under product code HQJ with a decision year between 1976 and 1989, 1988 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code HQJ by decision year
YearClearances
19761
19831
19882
19891

Applicants with the most clearances

Product code HQJ
Applicants holding the most 510(k) clearances under product code HQJ
ApplicantClearances
Acces Intl. Eyewear1
Bausch & Lomb Pharmaceutical, Inc.1
Bcd Products, Inc.1
Labtician Products, Inc.1
Medical Instrument Research Assoc., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code