FDA applicant

Howard K. Mann & Assoc.

Edison, NJ1 decision1995–19950 recalls

FDA records 1 decision for Howard K. Mann & Assoc. (Edison, NJ) in 1995: 1 510(k) clearance. All are in product code CAF (Nebulizer (Direct Patient Interface)). 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, anesthesiology panel, where it files most

How often FDA has decided Howard K. Mann & Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Howard K. Mann & Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Howard K. Mann & Assoc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Howard”

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

Howard Instruments, Inc. 5 Howard Medical Co. 3 Howard Associates, Inc. 3 Howard, Hills & Harsh 2 Howard N. Amos Design & Mfg. 1 Howard J. Nethery & Assoc. 1

Howard K. Mann & Assoc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Howard”