SEJOY, MODEL MT-403
K-Number: K051699 · 2006-02-06
Advertisement
Device Summary
Frequently Asked Questions
What is the SEJOY, MODEL MT-403?
SEJOY, MODEL MT-403 is a medical device that received FDA 510(k) clearance on 2006-02-06. The listed applicant is Sejoy Electronics & Instruments Co., Ltd.. The 510(k) number is K051699.
When did SEJOY, MODEL MT-403 receive FDA 510(k) clearance?
SEJOY, MODEL MT-403 received FDA 510(k) clearance on 2006-02-06, under 510(k) number K051699.
Who is the listed applicant for SEJOY, MODEL MT-403?
The FDA 510(k) record lists Sejoy Electronics & Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEJOY, MODEL MT-403?
The FDA product code for SEJOY, MODEL MT-403 is FLL.
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 Sejoy Electronics & Instruments 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: FLL)
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.
Advertisement