510(k) Report

FDA applicant

Ab2 Medical Products, Llp

The Woodlands, TX1 decision1999–19990 recalls

FDA records 1 decision for Ab2 Medical Products, Llp (The Woodlands, TX) in 1999: 1 510(k) clearance. All are in product code FPA (Set, Administration, Intravascular). 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, general hospital panel, where it files most

How often FDA has decided Ab2 Medical Products, Llp’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ab2 Medical Products, Llp since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ab2 Medical Products, Llp by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ab2 Medical Products, Llp’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

Which product codes does it file in?

  • FPASet, Administration, Intravascular1decision

What has FDA decided for it lately?

  • K984569AB2 Med-Flo Solution SetAb2 Medical Products, Llp · 1999

The one decision as Ab2 Medical Products, Llp →