Cleared Traditional

K862728 - HOSKINS NYLON SUTURE LASER LENS

K862728 is the FDA 510(k) clearance for HOSKINS NYLON SUTURE LASER LENS by Ocular Instruments, Inc.. It is a Class 2 Ophthalmic device (product code HJK) cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K862728 · Ocular Instruments, Inc. · Ophthalmic device
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Aug 1986
Decision
34d
Days
Class 2
Risk

K862728 is an FDA 510(k) clearance for the HOSKINS NYLON SUTURE LASER LENS. Classified as Lens, Contact, Polymethylmethacrylate, Diagnostic (product code HJK), Class II - Special Controls.

Submitted by Ocular Instruments, Inc. (Bellevue, US). The FDA issued a Cleared decision on August 21, 1986 after a review of 34 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 Ocular Instruments, Inc. devices

Submission Details

510(k) Number K862728 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 18, 1986
Decision Date August 21, 1986
Days to Decision 34 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 110d · This submission: 34d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 27
Devices cleared under the same product code (HJK) and FDA review panel - the closest regulatory comparables to K862728.
YANNUZZI FUNDUS LASER LENS
K864304 · Ocular Instruments, Inc. · Dec 1986
MAINSTER RETINA LASER LENS
K863911 · Ocular Instruments, Inc. · Dec 1986
LANDERS INDIRECT VITRECTOMY LENS
K864418 · Ocular Instruments, Inc. · Nov 1986
ABRAHAM YAG LASER LENS
K862868 · Ocular Instruments, Inc. · Aug 1986
SCHIRMER PERIPHERAL IRIDECTOMY LASER LENS
K863027 · Ocular Instruments, Inc. · Aug 1986
WISE IRIDOTOMY-SPINCTEROTOMY LENS
K861648 · Ocular Instruments, Inc. · Jun 1986