FDA applicant

Professional Medical Device Consultants

Sandy, UT1 decision1995–199531 recalls

FDA records 1 decision for Professional Medical Device Consultants (Sandy, UT) in 1995: 1 510(k) clearance. All are in product code CAZ (Anesthesia Conduction Kit). 31 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, anesthesiology panel, where it files most

How often FDA has decided Professional Medical Device Consultants’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Professional Medical Device Consultants since 2007.

Recalls per year

1in 2013

2007high 29 (2009) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Professional Medical Device Consultants by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Professional Medical Device Consultants’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 “Professional”

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

Professional Medical Services 19 Professional Medical Products, Inc. 9 Professional Latex Sdn Bhd 3 Professional Instruments Co. 3 Professional Positioners, Inc. 3 Professional Tape Co., Inc. 2 Professional Services For Surgeons, Ltd. 2 Professional Dental Mfg., Inc. 2 Professional Technologies Corp. 2 Professional Supplies, Inc. 2 Professional Disposables International, Inc. 1 Professional Medical Systems 1

Professional Medical Device Consultants

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Professional”