iVitri Straw
K-Number: K172751 · 2018-02-09
Device Summary
Frequently Asked Questions
What is the iVitri Straw?
iVitri Straw is a medical device that received FDA 510(k) clearance on 2018-02-09. The listed applicant is Reprobitech Corp.. The 510(k) number is K172751.
When did iVitri Straw receive FDA 510(k) clearance?
iVitri Straw received FDA 510(k) clearance on 2018-02-09, under 510(k) number K172751.
Who is the listed applicant for iVitri Straw?
The FDA 510(k) record lists Reprobitech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iVitri Straw?
The FDA product code for iVitri Straw is MQK.
Other records listing Reprobitech Corp. 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: MQK)
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.