# K990547: Pilling Weck Surgical Y Stent Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Pilling Weck, Inc.
- Decided: Apr 27, 1999 after 64 days
- Product code: EOQ (Bronchoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4680
- 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. The FDA summary names its predicate without a number.
- (no number) Karl Storz Stent Applicator Forceps: named in the summary without a submission number

## Indications for use
The Pilling Weck Surgical Y Stent Forceps (Bronchoscope (Flexible or Rigid) is to inset tracheobronchial stents during ENT procedures

Source page: https://510kreport.com/device/K990547
Methodology: https://510kreport.com/methodology