FDA applicant

Access Devices, Inc.

Chadds Ford, PA3 decisions1982–19830 recalls

FDA records 3 decisions for Access Devices, Inc. (Chadds Ford, PA) from 1982 to 1983: 3 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and DYB (Introducer, Catheter). 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 Access Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Access Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Point Medical, LLC 4 Access Bio Incorporate 4 Access Bio, 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 Devices, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Access”