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. The listed applicant is Pentax of America, Inc.. The 510(k) number is K173679.
When did PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes receive FDA 510(k) clearance?
PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes received FDA 510(k) clearance on 2018-07-03, under 510(k) number K173679.
Who is the listed applicant for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
The FDA 510(k) record lists Pentax of America, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Pentax of America, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: PEA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.