Non-Sterile Ultrasound Gel Sterile Ultrasound Gel
K-Number: K253255 · 2026-06-17
Device Summary
Frequently Asked Questions
What is the Non-Sterile Ultrasound Gel Sterile Ultrasound Gel?
Non-Sterile Ultrasound Gel Sterile Ultrasound Gel is a medical device that received FDA 510(k) clearance on 2026-06-17. The listed applicant is Foshan Pingchuang Medical Technology Co., Ltd.. The 510(k) number is K253255.
When did Non-Sterile Ultrasound Gel Sterile Ultrasound Gel receive FDA 510(k) clearance?
Non-Sterile Ultrasound Gel Sterile Ultrasound Gel received FDA 510(k) clearance on 2026-06-17, under 510(k) number K253255.
Who is the listed applicant for Non-Sterile Ultrasound Gel Sterile Ultrasound Gel?
The FDA 510(k) record lists Foshan Pingchuang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Non-Sterile Ultrasound Gel Sterile Ultrasound Gel?
The FDA product code for Non-Sterile Ultrasound Gel Sterile Ultrasound Gel is MUI.
Related Clinical Trials
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.
Other records listing Foshan Pingchuang Medical Technology Co., Ltd. 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: MUI)
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.