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FDA 510(k)

FUJIFILM Video Laparoscope

K-Number: K202130 · 2020-08-20

ApplicantFujifilm Corporation
Decision Date2020-08-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Video Laparoscope is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2020-08-20 under approval number K202130. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJIFILM Video Laparoscope?

FUJIFILM Video Laparoscope is a medical device that received FDA 510(k) clearance on 2020-08-20. It is manufactured by Fujifilm Corporation. The 510(k) number is K202130.

When was FUJIFILM Video Laparoscope approved by the FDA?

FUJIFILM Video Laparoscope received FDA 510(k) clearance on 2020-08-20, under approval number K202130.

What company makes FUJIFILM Video Laparoscope?

FUJIFILM Video Laparoscope is manufactured by Fujifilm Corporation.

What is the FDA product code for FUJIFILM Video Laparoscope?

The FDA product code for FUJIFILM Video Laparoscope is GCJ.

Other Devices by Fujifilm Corporation

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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