MMN-1 COARSE MANIPULATOR
K-Number: K002653 · 2000-09-22
Advertisement
Device Summary
Frequently Asked Questions
What is the MMN-1 COARSE MANIPULATOR?
MMN-1 COARSE MANIPULATOR is a medical device that received FDA 510(k) clearance on 2000-09-22. The listed applicant is Narishige Co., Ltd.. The 510(k) number is K002653.
When did MMN-1 COARSE MANIPULATOR receive FDA 510(k) clearance?
MMN-1 COARSE MANIPULATOR received FDA 510(k) clearance on 2000-09-22, under 510(k) number K002653.
Who is the listed applicant for MMN-1 COARSE MANIPULATOR?
The FDA 510(k) record lists Narishige Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MMN-1 COARSE MANIPULATOR?
The FDA product code for MMN-1 COARSE MANIPULATOR is MQJ.
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 Narishige 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: MQJ)
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