FDA applicant

Richard D. Spradlin

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Richard D. Spradlin (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code KXJ (Table, Radiologic). 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 Richard D. Spradlin’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Richard D. Spradlin since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Richard”

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

Richard Wolf Medical Instruments Corp. 155 Richard'S Medical Equip., Inc. 48 Richard-Allan Medical Ind., Inc. 33 Richard-Allan Medical 8 Richard Hamer Assoc., Inc. 8 Richard F. Kronner, M.D. 3 Richard James, Inc. 2 Richard Ting 1 Richard Scott Elliott 1 Richard G. Deniro 1 Richard R. Anthony, M.D. 1 Richard J. Turner Assoc. 1

Richard D. Spradlin

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Richard”