Cleared Traditional

SUMMIT OPTICS CONTACT LENS REMOVER (K870072) - FDA 510(k) Clearance

Class I Ophthalmic device.

K870072 · Dayton Mfg. Co. · Ophthalmic device
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Feb 1987
Decision
35d
Days
Class 1
Risk

K870072 is an FDA 510(k) clearance for the SUMMIT OPTICS CONTACT LENS REMOVER. Classified as Inserter/remover Contact Lens (product code KYE), Class I - General Controls.

Submitted by Dayton Mfg. Co. (Tampa, US). The FDA issued a Cleared decision on February 12, 1987 after a review of 35 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5420 - 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 Dayton Mfg. Co. devices

Submission Details

510(k) Number K870072 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 1987
Decision Date February 12, 1987
Days to Decision 35 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 110d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KYE Inserter/remover Contact Lens
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5420
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.