FDA applicant

Deka Research & Development Corp.

Manchester, NH13 decisions1984–20251 recall

FDA records 13 decisions for Deka Research & Development Corp. (Manchester, NH) from 1984 to 2025: 13 510(k) clearances. Most are in product codes LDR (Controller, Infusion, Intravascular, Electronic) and FKX (System, Peritoneal, Automatic Delivery). Its devices cite 14 predicates, 4 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “DEKA Research & Development”.

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 Deka Research & Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2025

2007high 2 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2014

2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Deka Research & Development Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Deka Research & Development Corp.’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 “Deka”

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

Deka Research and Development 16 Deka Integrated Solutions Corporation 1 Deka R&D Corp 1

Deka Research & Development Corp.

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?

What has been recalled?

Other applicant names beginning “Deka”