510(k) Report

FDA applicant

Precise Optics Photo Medic Equipment, Inc.

Bay Shore, NY2 decisions1992–19920 recalls

FDA records 2 decisions for Precise Optics Photo Medic Equipment, Inc. (Bay Shore, NY) in 1992: 2 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Precise Optics Photo Medic Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Precise Optics Photo Medic Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Precise Optics Photo Medic Equipment, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Precise”

FDA records each applicant name separately; these may or may not be the same firm.