FDA applicant

Apollo Fluid Dynamics

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Apollo Fluid Dynamics (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code INX (Bed, Air Fluidized). 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, physical medicine panel, where it files most

How often FDA has decided Apollo Fluid Dynamics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Apollo Fluid Dynamics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Apollo”

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

Apollo Endosurgery, Inc. 14 Apollo Spine, Inc. 7 Apollo Enterprise, Ltd. Co. 3 Apollo Medical Imaging Technology Pty., Ltd. 2 Apollo Dental Products, Inc. 2 Apollo Products, Inc. 1 Apollo'S Suntanning Supplies 1 Apollo Medical Optics, Ltd. 1 Apollo Corp. 1 Apollo Physical Therapy Products International 1

Apollo Fluid Dynamics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Apollo”