Quickie(r) Q700-UP M
K-Number: K172384 · 2018-01-16
Device Summary
Frequently Asked Questions
What is the Quickie(r) Q700-UP M?
Quickie(r) Q700-UP M is a medical device that received FDA 510(k) clearance on 2018-01-16. The listed applicant is Sunrise Medical (Us), LLC. The 510(k) number is K172384.
When did Quickie(r) Q700-UP M receive FDA 510(k) clearance?
Quickie(r) Q700-UP M received FDA 510(k) clearance on 2018-01-16, under 510(k) number K172384.
Who is the listed applicant for Quickie(r) Q700-UP M?
The FDA 510(k) record lists Sunrise Medical (Us), LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Quickie(r) Q700-UP M?
The FDA product code for Quickie(r) Q700-UP M is IPL.
Other records listing Sunrise Medical (Us), LLC 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: IPL)
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.