510(k) Report

FDA applicant

Absentee Shawnee Bandage Group

Tecumseh, OK3 decisions1993–19930 recalls

FDA records 3 decisions for Absentee Shawnee Bandage Group (Tecumseh, OK) in 1993: 3 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and LRR (First Aid Kit With Drug). 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 Absentee Shawnee Bandage Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Absentee Shawnee Bandage Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Absentee Shawnee Bandage Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Absentee Shawnee Bandage Group’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