PicoSure Workstation
K-Number: K173199 · 2018-02-07
Device Summary
Frequently Asked Questions
What is the PicoSure Workstation?
PicoSure Workstation is a medical device that received FDA 510(k) clearance on 2018-02-07. The listed applicant is Cynosure, Inc.. The 510(k) number is K173199.
When did PicoSure Workstation receive FDA 510(k) clearance?
PicoSure Workstation received FDA 510(k) clearance on 2018-02-07, under 510(k) number K173199.
Who is the listed applicant for PicoSure Workstation?
The FDA 510(k) record lists Cynosure, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PicoSure Workstation?
The FDA product code for PicoSure Workstation is GEX. This falls under the Gastroenterology category.
Other records listing Cynosure, 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: GEX)
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.