510(k) Report

FDA applicant

Advanced Clinical Products, Inc.

Richmond, VA4 decisions1986–19871 recall

FDA records 4 decisions for Advanced Clinical Products, Inc. (Richmond, VA) from 1986 to 1987: 4 510(k) clearances. All are in product code KNX (Collector, Urine, (And Accessories) For…). 1 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 Advanced Clinical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Clinical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • KNXCollector, Urine, (And Accessories) For Indwelling Catheter4decisions

What has FDA decided for it lately?

  • K871387Second Nature (TM)Advanced Clinical Products, Inc. · 19871 recall
  • K862581Nephrostomy Connecting Tube (a-50)Advanced Clinical Products, Inc. · 1986
  • K862580Nephrostomy Drainage Kit (a-150)Advanced Clinical Products, Inc. · 1986
  • K861192Gentle Back, Plastic Urinary Drainage BagAdvanced Clinical Products, Inc. · 1986

All 4 as Advanced Clinical Products, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K871387Latex-Free REF B1000, Belly Bag Urine Collection Bag with Hip Belt, ***1000 ml…May 13, 2004