PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes
K-Number: K173679 · 2018-07-03
Device Summary
Frequently Asked Questions
What is the PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is a medical device that received FDA 510(k) clearance on 2018-07-03. It is manufactured by Pentax of America, Inc.. The 510(k) number is K173679.
When was PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes approved by the FDA?
PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes received FDA 510(k) clearance on 2018-07-03, under approval number K173679.
What company makes PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is manufactured by Pentax of America, Inc..
What is the FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
The FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is PEA.
Related Clinical Trials
Related PubMed Literature
Other Devices by Pentax of America, Inc.
Related Devices (Code: PEA)
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.