FDA applicant

Appasamy Associates (U.S.A.), Inc.

Millersville, MD1 decision1994–19940 recalls

FDA records 1 decision for Appasamy Associates (U.S.A.), Inc. (Millersville, MD) in 1994: 1 510(k) clearance. All are in product code FSO (Microscope, Surgical, General & Plastic Surgery). 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 and plastic surgery panel, where it files most

How often FDA has decided Appasamy Associates (U.S.A.), Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Appasamy Associates (U.S.A.), Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Appasamy Associates (U.S.A.), Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Appasamy Associates (U.S.A.), Inc.’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 “Appasamy”

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

Appasamy Associates 2

Appasamy Associates (U.S.A.), Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Appasamy”