510(k) Report

FDA applicant

Central Georgia Ancillary Health Systems

Macon, GA3 decisions1991–19930 recalls

FDA records 3 decisions for Central Georgia Ancillary Health Systems (Macon, GA) from 1991 to 1993: 3 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and FZI (Apparatus, Air Handling, Enclosure). 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 and plastic surgery panel, where it files most

How often FDA has decided Central Georgia Ancillary Health Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Central Georgia Ancillary Health Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Central Georgia Ancillary Health Systems by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Central Georgia Ancillary Health Systems’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?

  • KKXDrape, Surgical, Antimicrobial2decisions
  • FZIApparatus, Air Handling, Enclosure1decision

What has FDA decided for it lately?

  • K923798Surgical Gown PackCentral Georgia Ancillary Health Systems · 1993
  • K911131Sterile Surgical Gown PackCentral Georgia Ancillary Health Systems · 1991
  • K911132Multiple, Surgical Drape PackCentral Georgia Ancillary Health Systems · 1991

All 3 as Central Georgia Ancillary Health Systems →