FDA applicant

P.T. Panca Pusaka Deli

Chester, NY1 decision1998–19980 recalls

FDA records 1 decision for P.T. Panca Pusaka Deli (Chester, NY) in 1998: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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 P.T. Panca Pusaka Deli’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for P.T. Panca Pusaka Deli since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — P.T. Panca Pusaka Deli by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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P.T. Panca Pusaka Deli

Which product codes does it file in?

What has FDA decided for it lately?