Pilling Weck Surgical Y Stent Forceps

K990547 is the FDA 510(k) clearance record for PILLING WECK SURGICAL Y STENT FORCEPS, a class II device, cleared for Pilling Weck, Inc. on 1999-04-27 under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)). FDA's definition for product code EOQ reads: "A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the...". FDA records list 6 510(k) clearances for Pilling Weck, Inc., from 1994-08-24 to 1999-04-27. As of 2026-09-10, FDA records show no recalls naming K990547.