FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01
K-Number: K223827 · 2023-09-08
ApplicantFujifilm Corporation
Decision Date2023-09-08
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01 is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2023-09-08 under approval number K223827. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01?
FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01 is a medical device that received FDA 510(k) clearance on 2023-09-08. It is manufactured by Fujifilm Corporation. The 510(k) number is K223827.
When was FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01 approved by the FDA?
FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01 received FDA 510(k) clearance on 2023-09-08, under approval number K223827.
What company makes FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01?
FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01 is manufactured by Fujifilm Corporation.
What is the FDA product code for FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01?
The FDA product code for FUJIFILM Endoscope Model EC-760S-A/L, Endoscopy Support Program EW10-VM01 is FDF.
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Official Source
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