Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: FSO FDA class 1

Microscope, Surgical, General & Plastic Surgery

General, Plastic Surgery

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A surgical microscope for general and plastic surgery is an optical instrument providing high magnification and illumination, used to enable precise visualization during delicate operative procedures. It is classified as FDA Class 1 (lowest risk), subject to general controls only, and does not require premarket notification. The product code is FSO, regulated under 21 CFR 878.4700, within the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

15 matches
K Number
Device Name
MICROFLEX
OPERATING MICROSCOPE AA OM 10
DEEMED MSS -- MICROSCOPE SUPPORT SYSTEM
SOM 6VI (SURGICAL OPERATING MICROSCOPE)
WOODLYN OPERATION MICROSCOPE
MOLLER-WEDEL OPERATING MICROSCOPE
SOM 6V
J2 MICROSCOPE
OPMI MD SURGICAL MICROSCOPE
ODONTO-SCOPE
BINOCULAR OPER. MICROSCOPES & ACCESSOR
BINOCULAR OPERATING MICROSCOPES AND
FMS-02 FLOOR-UNIT MODEL MICROSCOPE
VOCON MODEL VC526
OPERATION MICROSCOPE SOM 1

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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