Cleared Traditional

K872747 - LASER CENTERING DEVICE (FDA 510(k) Clearance)

Class I Ophthalmic device.

K872747 · Innomed Corp. · Ophthalmic device
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Sep 1987
Decision
53d
Days
Class 1
Risk

K872747 is an FDA 510(k) clearance for the LASER CENTERING DEVICE. Classified as Marker, Ocular (product code HMR), Class I - General Controls.

Submitted by Innomed Corp. (Brea, US). The FDA issued a Cleared decision on September 4, 1987 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4570 - 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 Innomed Corp. devices

Submission Details

510(k) Number K872747 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 1987
Decision Date September 04, 1987
Days to Decision 53 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
57d faster than avg
Panel avg: 110d · This submission: 53d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HMR Marker, Ocular
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4570
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.