FDA applicant

Access Point Medical, LLC

Potomac, MD4 decisions2005–20070 recalls

FDA records 4 decisions for Access Point Medical, LLC (Potomac, MD) from 2005 to 2007: 4 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) and CAF (Nebulizer (Direct Patient Interface)). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 Access Point Medical, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Access Point Medical, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Access Point Medical, LLC’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 “Access”

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

Access Scientific, Inc. 14 Access Surgical Intl., Inc. 9 Access Vascular, Inc. 9 Access / God Loves You 4 Access Bio Incorporate 4 Access Bio, Inc. 3 Access Devices, Inc. 3 Access Pharmaceuticals, Inc. 2 Access Battery, Inc. 2 Access Radiology Corp. 2 Access Cardiosystems, Inc. 2 Access Point Technologies Ep, Inc. 1

Access Point Medical, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Access”