# K993033: Intray GC

- Pathway: 510(k) (Traditional)
- Applicant: Biomed Diagnostics, Inc.
- Decided: Dec 16, 1999 after 98 days
- Product code: JTY (Culture Media, For Isolation Of Pathogenic Neisseria)
- Device class: 2
- Regulation: 21 CFR 866.2410
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K210511: InTray GC (2021), 0 descendants of its own

## Indications for use
InTray GC is used, like conventional Thayer-Martin media plates, to grow Neisseria gonomhoeae and similar organisms.

Source page: https://510kreport.com/device/K993033
Methodology: https://510kreport.com/methodology