Cleared Traditional

K851262 - AMER. MEDICAL OPTICAL BINOCULAR INDIRECT OPHTHALMA

K851262 is an FDA 510(k) clearance for AMER. MEDICAL OPTICAL BINOCULAR INDIREC..., manufactured by American Medical Optics. The device is a Class 2 Ophthalmic device with product code HLI cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K851262 · American Medical Optics · Ophthalmic device
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Apr 1985
Decision
33d
Days
Class 2
Risk

K851262 is an FDA 510(k) clearance for the AMER. MEDICAL OPTICAL BINOCULAR INDIRECT OPHTHALMA. Classified as Ophthalmoscope, Ac-powered (product code HLI), Class II - Special Controls.

Submitted by American Medical Optics (Irvine, US). The FDA issued a Cleared decision on April 30, 1985 after a review of 33 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.1570 - 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 American Medical Optics devices

FDA 510(k) Submission Details - K851262

510(k) Number K851262 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 28, 1985
Decision Date April 30, 1985
Days to Decision 33 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
77d faster than avg
Panel avg: 110d · This submission: 33d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HLI Device Classification - Class 2, Special Controls

Product Code HLI Ophthalmoscope, Ac-powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.1570
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 - HLI Ophthalmoscope, Ac-powered

All 56
Devices cleared under the same product code (HLI) and FDA review panel - the closest regulatory comparables to K851262.
THE KEELER ALL PUPIL INDIRECT OPHTHALMOSCOPE
K854244 · Keeler Instruments, Inc. · Nov 1985
AMER. MEDICAL OPTIC MONOCULAR DIRECT OPHTHALMASCOP
K851263 · American Medical Optics · May 1985
AMER. MEDICAL OPTICS MONOCULAR INDIRECT OPHTHALMAS
K851264 · American Medical Optics · May 1985
NIDEK-BINOCULAR INDIRECT OPHTHALMOSCOPE
K843596 · Nidek, Inc. · Feb 1985
NIDEK MONOCULAR INDIRECT OPHTHALMOSCOPE
K843597 · Nidek, Inc. · Feb 1985
MONOCULAR DIRECT OPHTHALMOSCOPE
K844971 · Nidek, Inc. · Feb 1985