Cleared Traditional

K062259 - ISCIENCE SURGICAL FIBEROPTIC ILLUMINATOR, MODEL FI - 100

K062259 is an FDA 510(k) clearance for ISCIENCE SURGICAL FIBEROPTIC ILLUMINATOR, manufactured by Iscience Surgical. The device is a Class 2 Ophthalmic device with product code MPA cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K062259 · Iscience Surgical · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2006
Decision
11d
Days
Class 2
Risk

K062259 is an FDA 510(k) clearance for the ISCIENCE SURGICAL FIBEROPTIC ILLUMINATOR, MODEL FI - 100. Classified as Endoilluminator (product code MPA), Class II - Special Controls.

Submitted by Iscience Surgical (Menlo Park, US). The FDA issued a Cleared decision on August 15, 2006 after a review of 11 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 876.1500 - 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 Iscience Surgical devices

FDA 510(k) Submission Details - K062259

510(k) Number K062259 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 2006
Decision Date August 15, 2006
Days to Decision 11 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 110d · This submission: 11d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

MPA Device Classification - Class 2, Special Controls

Product Code MPA Endoilluminator
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
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 - MPA Endoilluminator

All 30
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