FDA applicant

Howard Associates, Inc.

Astoria, NY3 decisions1986–19900 recalls

FDA records 3 decisions for Howard Associates, Inc. (Astoria, NY) from 1986 to 1990: 3 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). 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 Howard Associates, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Howard Associates, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Howard Associates, Inc. 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, Hills & Harsh 2 Howard K. Mann & Assoc. 1 Howard N. Amos Design & Mfg. 1 Howard J. Nethery & Assoc. 1

Howard Associates, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Howard”