FDA applicant

Berman, Pcp & Consultants, Inc.

Mchenry, IL7 decisions1977–19780 recalls

FDA records 7 decisions for Berman, Pcp & Consultants, Inc. (Mchenry, IL) from 1977 to 1978: 7 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FPK (Tubing, Fluid Delivery). 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 Berman, Pcp & Consultants, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Berman, Pcp & Consultants, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Berman, Pcp & Consultants, 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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Berman, Pcp & Consultants, Inc.

Which product codes does it file in?

What has FDA decided for it lately?