Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702
K-Number: K202937 · 2021-03-18
Device Summary
Frequently Asked Questions
What is the Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702?
Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702 is a medical device that received FDA 510(k) clearance on 2021-03-18. The listed applicant is Ceragem Co., Ltd.. The 510(k) number is K202937.
When did Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702 receive FDA 510(k) clearance?
Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702 received FDA 510(k) clearance on 2021-03-18, under 510(k) number K202937.
Who is the listed applicant for Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702?
The FDA 510(k) record lists Ceragem Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702?
The FDA product code for Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702 is JFB.
Other records listing Ceragem 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: JFB)
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.