FDA applicant

Millar Instruments, Inc.

Houston, TX18 decisions1979–20113 recalls

FDA records 18 decisions for Millar Instruments, Inc. (Houston, TX) from 1979 to 2011: 18 510(k) clearances. Most are in product codes DXO (Transducer, Pressure, Catheter Tip) and DQO (Catheter, Intravascular, Diagnostic). Its devices cite 3 predicates, 2 of them its own earlier devices. 3 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 Millar Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2011

2007high 1 (2010) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Millar Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Millar Instruments, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Millar”

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

Millar, Inc. 1

Millar Instruments, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

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Other applicant names beginning “Millar”