# K030525: Custom Products Ivf Workstation Type WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 and WKST-24*72D Plus Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Mid-Atlantic Diagnostics, Inc.
- Decided: Aug 27, 2003 after 189 days
- Product code: MQG (Accessory, Assisted Reproduction)
- Device class: 2
- Regulation: 21 CFR 884.6120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Mid-Atlantic Diagnostics Custom Products IVF Workstation is a laminar flow hood that is indicated for use as an accessory to assisted reproduction technologies/in vitro fertilization (ART/IVF) procedures.

Source page: https://510kreport.com/device/K030525
Methodology: https://510kreport.com/methodology