# K990738: DR. Jahanger's Cutter

- Pathway: 510(k) (Traditional)
- Applicant: M.S. Jahanger, MD
- Decided: Oct 29, 1999 after 238 days
- Product code: KNA (Instrument, Manual, Specialized Obstetric-Gynecologic)
- Device class: 2
- Regulation: 21 CFR 884.4530
- 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
This instrument will be used to cut and clamp the umbilical cord in normal and abnormal deliveries. The instrument will cut and clamp both mother’s side and baby’s side of the unuvilical cord, simultaneously.

Source page: https://510kreport.com/device/K990738
Methodology: https://510kreport.com/methodology