FDA applicant

Emergency Medicine

Library, PA1 decision1981–19810 recalls

FDA records 1 decision for Emergency Medicine (Library, PA) in 1981: 1 510(k) clearance. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Emergency Medicine’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Emergency Medicine since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Emergency Medicine’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 “Emergency”

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

Emergency Filtration Products, Inc. 2 Emergency Situation Products 2 Emergency Medical Techology 1 Emergency Medical Supply, Inc. 1 Emergency Management Products, Inc. 1 Emergency Medical Devices, LLC 1 Emergency Products and Research 1

Emergency Medicine

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Emergency”