Cleared Traditional

K030054 - DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES

K030054 is an FDA 510(k) clearance for DISPOSABLE VITRECTOMY SETS, manufactured by Fci Ophthalmics, Inc.. The device is a Class 2 Ophthalmic device with product code HJK cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K030054 · Fci Ophthalmics, Inc. · Ophthalmic device
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Feb 2003
Decision
51d
Days
Class 2
Risk

K030054 is an FDA 510(k) clearance for the DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES. Classified as Lens, Contact, Polymethylmethacrylate, Diagnostic (product code HJK), Class II - Special Controls.

Submitted by Fci Ophthalmics, Inc. (Centercille, US). The FDA issued a Cleared decision on February 26, 2003 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.1385 - the FDA ophthalmic device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Fci Ophthalmics, Inc. devices

FDA 510(k) Submission Details - K030054

510(k) Number K030054 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 06, 2003
Decision Date February 26, 2003
Days to Decision 51 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 110d · This submission: 51d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HJK Device Classification - Class 2, Special Controls

Product Code HJK Lens, Contact, Polymethylmethacrylate, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.1385
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Ophthalmic devices follow this clearance model.

Regulatory Peers - HJK Lens, Contact, Polymethylmethacrylate, Diagnostic

All 29
Devices cleared under the same product code (HJK) and FDA review panel - the closest regulatory comparables to K030054.
RxSight Contact Lens
K201909 · Rxsight, Inc. · Sep 2020
Endocular Viewing Lenses and Silicone Ring
K173944 · Phakos · Oct 2018
STAURENGHI WIDE FIELD SCANNING LASER LENS
K014170 · Ocular Instruments, Inc. · Mar 2002
DISPOSABLE VITRECTOMY LENS
K012096 · Ocular Instruments, Inc. · Aug 2001
ENDOVIEW SPPHIRE LENS SET
K971853 · American Medical Devices, Inc. · Aug 1997
MANDELKORN SUTURE LYSIS LENS
K933976 · Ocular Instruments, Inc. · Nov 1994