Kaiser No Cannula Thoracoscopy/Laparoscopy Instr

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K925198 ↗

FDA Product Code

GCJ

Device Class

Class II

Regulation

21 CFR Part 876.1500

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Pilling Identiloops

  Not classified

  FDA 510(k) K854914 Active Cleared 24 Jan 1986

• Pilling Laparoscopic Instrumentation

  Class II

  FDA 510(k) K934427 Active Cleared 10 Jan 1994

• Arterial Graft Sizers

  Not classified

  FDA 510(k) K761141 Active Cleared 6 Jan 1977

• Frazier Suction Instrument-Dispos

  Class I

  FDA 510(k) K832636 Active Cleared 14 Oct 1983

• Fiberbronchoscope (Pentax Fb-17A)

  Class II

  FDA 510(k) K760171 Active Cleared 19 Jul 1976

• Laser Bronchoscope System

  Class II

  FDA 510(k) K861921 Active Cleared 2 Jun 1986

See all devices from Pilling Co. →

• What is the Kaiser No Cannula Thoracoscopy/Laparoscopy Instrument used for?

  The Kaiser No Cannula Thoracoscopy/Laparoscopy Instrument is designed for diagnostic and surgical applications in the thoracic and abdominal cavities, intended for use in general and plastic surgery, gastroenterology, and urology procedures.

• Is the Kaiser No Cannula Thoracoscopy/Laparoscopy Instrument reusable or single-use?

  This device is supplied as a reusable instrument, meaning it can be cleaned and sterilized for multiple uses according to the manufacturer's instructions.

• What are the regulatory approvals for the Kaiser No Cannula Thoracoscopy/Laparoscopy Instrument?

  The device is authorized under FDA 510K clearance with product code GCJ and model number K925198, having been determined substantially equivalent to predicate devices.

• Who manufactures the Kaiser No Cannula Thoracoscopy/Laparoscopy Instrument?

  The Kaiser No Cannula Thoracoscopy/Laparoscopy Instrument is manufactured by Pilling Co., located in Fort Washington, PA, with Richard G Jones as the contact person.