GoBack Crossing Catheter
K-Number: K211802 · 2022-03-01
Decision Date2022-03-01
Product CodePDU
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
GoBack Crossing Catheter is a medical device manufactured by Upstream Peripheral Technologies, Ltd.. It received FDA 510(k) clearance on 2022-03-01 under approval number K211802. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the GoBack Crossing Catheter?
GoBack Crossing Catheter is a medical device that received FDA 510(k) clearance on 2022-03-01. It is manufactured by Upstream Peripheral Technologies, Ltd.. The 510(k) number is K211802.
When was GoBack Crossing Catheter approved by the FDA?
GoBack Crossing Catheter received FDA 510(k) clearance on 2022-03-01, under approval number K211802.
What company makes GoBack Crossing Catheter?
GoBack Crossing Catheter is manufactured by Upstream Peripheral Technologies, Ltd..
What is the FDA product code for GoBack Crossing Catheter?
The FDA product code for GoBack Crossing Catheter is PDU.
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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.