MICROMANIPULATOR SET
K-Number: K120877 · 2012-06-20
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Device Summary
Frequently Asked Questions
What is the MICROMANIPULATOR SET?
MICROMANIPULATOR SET is a medical device that received FDA 510(k) clearance on 2012-06-20. The listed applicant is Narishige Co., Ltd.. The 510(k) number is K120877.
When did MICROMANIPULATOR SET receive FDA 510(k) clearance?
MICROMANIPULATOR SET received FDA 510(k) clearance on 2012-06-20, under 510(k) number K120877.
Who is the listed applicant for MICROMANIPULATOR SET?
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 MICROMANIPULATOR SET?
The FDA product code for MICROMANIPULATOR SET 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.
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