Cleared Traditional

K896072 - D.L. SCOPE OPHTHALMOSCOPE

K896072 is an FDA 510(k) clearance for D.L. SCOPE OPHTHALMOSCOPE, manufactured by North American Medical Products, Inc.. The device is a Class 2 Ophthalmic device with product code HLJ cleared through the Traditional 510(k) pathway after a 39-day FDA review.

K896072 · North American Medical Products, Inc. · Ophthalmic device
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Nov 1989
Decision
39d
Days
Class 2
Risk

K896072 is an FDA 510(k) clearance for the D.L. SCOPE OPHTHALMOSCOPE. Classified as Ophthalmoscope, Battery-powered (product code HLJ), Class II - Special Controls.

Submitted by North American Medical Products, Inc. (Loudonville, US). The FDA issued a Cleared decision on November 27, 1989 after a review of 39 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 North American Medical Products, Inc. devices

FDA 510(k) Submission Details - K896072

510(k) Number K896072 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 19, 1989
Decision Date November 27, 1989
Days to Decision 39 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 110d · This submission: 39d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HLJ Device Classification - Class 2, Special Controls

Product Code HLJ Ophthalmoscope, Battery-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 - HLJ Ophthalmoscope, Battery-powered

All 30
Devices cleared under the same product code (HLJ) and FDA review panel - the closest regulatory comparables to K896072.
RI-FORMER
K932504 · Rudolf Riester GmbH & Co. KG · Oct 1993
OPHTHALMOSCOPE
K925757 · Rudolf Riester GmbH & Co. KG · Aug 1993
MIS
K923543 · Ceram Optec, Inc. · Mar 1993
INDIRECT OPHTHALMOSCOPE
K853891 · Carl Zeiss, Inc. · Oct 1985
MEDIC LUX DIAGNOSTIC SETS
K832437 · Keeler Instruments, Inc. · Aug 1983
DORC LIGHTWEIGHT BINOCULAR OPHTHALMOSCOP
K830215 · Jedmed Instrument Co. · Mar 1983