510(k) Report

FDA applicant

Schiff Photo Mechanics

Mchenry, IL2 decisions1983–19830 recalls

FDA records 2 decisions for Schiff Photo Mechanics (Mchenry, IL) in 1983: 2 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and JAK (System, X-Ray, Tomography, Computed). 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 Schiff Photo Mechanics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Schiff Photo Mechanics since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Schiff Photo Mechanics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Schiff Photo Mechanics’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Schiff”

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