Cleared Traditional

K850532 - ATLANTIC OPTICAL SYSTEMS, INC. UNIVERSAL PACK

K850532 is an FDA 510(k) clearance for ATLANTIC OPTICAL SYSTEMS, manufactured by Atlantic Optical Systems, Inc.. The device is a Class 2 Ophthalmic device with product code HQC cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K850532 · Atlantic Optical Systems, Inc. · Ophthalmic device
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Apr 1985
Decision
63d
Days
Class 2
Risk

K850532 is an FDA 510(k) clearance for the ATLANTIC OPTICAL SYSTEMS, INC. UNIVERSAL PACK. Classified as Unit, Phacofragmentation (product code HQC), Class II - Special Controls.

Submitted by Atlantic Optical Systems, Inc. (Leechburg, US). The FDA issued a Cleared decision on April 15, 1985 after a review of 63 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4670 - 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 Atlantic Optical Systems, Inc. devices

FDA 510(k) Submission Details - K850532

510(k) Number K850532 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 11, 1985
Decision Date April 15, 1985
Days to Decision 63 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
47d faster than avg
Panel avg: 110d · This submission: 63d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HQC Device Classification - Class 2, Special Controls

Product Code HQC Unit, Phacofragmentation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.4670
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 - HQC Unit, Phacofragmentation

All 198
Devices cleared under the same product code (HQC) and FDA review panel - the closest regulatory comparables to K850532.
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INFUSION SLEEVE - OPHTHALMIC
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PHACO-BAC STOP KIT
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