FDA applicant

Apollo Products, Inc.

Walker, MI1 decision1979–19790 recalls

FDA records 1 decision for Apollo Products, Inc. (Walker, MI) in 1979: 1 510(k) clearance. All are in product code JOM (Plethysmograph, Photoelectric, Pneumatic Or…). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Apollo Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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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'S Suntanning Supplies 1 Apollo Medical Optics, Ltd. 1 Apollo Fluid Dynamics 1 Apollo Corp. 1 Apollo Physical Therapy Products International 1

Apollo Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Apollo”