Fujinon Video Laparoscope--Thoracoscopy

FDA 510(k) K931223 · Fujinon, Inc.

Substantially Equivalent

510(k) numberK931223

Submission

Device name
Fujinon Video Laparoscope--Thoracoscopy
Applicant
Fujinon, Inc.
New York, NY, US
Received
March 10, 1993
Decision date
July 28, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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More from TroCare, LLC

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K112391Fujinon ColonoscopesFDF · Special 07/26/2012SE
K102466Fujinon EPX-4440HD Digital Video ProcessorFET · Traditional 05/25/2011SE
K111243Fujinon Ultrasonic ProcessorFDS · Special 05/16/2011SE
K091773Fujinon Sterile OvertubesFED · Special 08/07/2009SE
K090116Fujinon Colonoscope for Double Balloon Enterscopy System Model, EC-450B15FDF · Traditional 04/22/2009SE
K063316Fujinon Model EG-530N Trans Nasal InsertionFDS · Traditional 03/16/2007SE
K063847Fujinon Ultrasonic Endoscope and Processor, Models EG-530UR, EG-530UT and SU-700FDS · Traditional 03/01/2007SE
K050907Fujinon G5 Bronchoscopes, Models EB-470S, EB-250S, and EB-270PEOQ · Traditional 05/19/2005SE
K042043Fujinon Inc. G5 Gastroscopes, Models EC-450WR5, EC-250WR5FDS · Traditional 11/24/2004SE

Questions and answers

When was Fujinon Video Laparoscope--Thoracoscopy cleared by the FDA?

Fujinon Video Laparoscope--Thoracoscopy (K931223) received a 510(k) decision of Substantially Equivalent on July 28, 1993, 140 days after the submission was received.

What is the product code of K931223?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.