FDA applicant

Transamerica Delaval, Inc.

Pasadena, CA7 decisions1984–198610 recalls

FDA records 7 decisions for Transamerica Delaval, Inc. (Pasadena, CA) from 1984 to 1986: 7 510(k) clearances. Most are in product codes DRS (Transducer, Blood-Pressure, Extravascular) and FMG (Stopcock, I.V. Set). 10 recalls are 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 Transamerica Delaval, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Transamerica Delaval, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Transamerica Delaval, 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 “Transamerica”

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

Transamerica Medical Systems 3 Transamerica Biomedical, Inc. 1 Transamerica Products, Inc. 1

Transamerica Delaval, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Transamerica”