FDA applicant

Hall/Mccollum Laboratories, Inc.

Charlottesville, VA2 decisions1986–19860 recalls

FDA records 2 decisions for Hall/Mccollum Laboratories, Inc. (Charlottesville, VA) in 1986: 2 510(k) clearances. All are in product code KOD (Catheter, Urological). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Hall/Mccollum Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hall/Mccollum 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 “Hall/Mccollum”

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

Hall Surgical, Division of Zimmer, Inc. 8 Hall Laboratories, Inc. 2 Hall-Woodroof, Inc. 2 Hall-Tech 2 Hall Medical Laboratories 2

Hall/Mccollum Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hall/Mccollum”