# K871998: Groshong CV Catheter Repair Kit

- Pathway: 510(k) (Traditional)
- Applicant: Catheter Technology Corp.
- Decided: Jun 24, 1987 after 29 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Jan 4, 2023 · Class II · Z-1051-2023: Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable).

Source page: https://510kreport.com/device/K871998
Methodology: https://510kreport.com/methodology