FDA applicant

Palco Laboratories, Inc.

Santa Cruz, CA9 decisions1983–19950 recalls

FDA records 9 decisions for Palco Laboratories, Inc. (Santa Cruz, CA) from 1983 to 1995: 9 510(k) clearances. Most are in product codes DQA (Oximeter) and 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, cardiovascular panel, where it files most

How often FDA has decided Palco Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Palco Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Palco Laboratories, 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 “Palco”

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

Palco Labs, Inc. 2

Palco Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Palco”