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FDA 510(k)

MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR

K-Number: K003298 · 2000-11-21

Decision Date2000-11-21
Product CodeMQJ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Narishige Co., Ltd.. It received FDA 510(k) clearance on 2000-11-21 under 510(k) number K003298. The device is classified under product code MQJ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR?

MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR is a medical device that received FDA 510(k) clearance on 2000-11-21. The listed applicant is Narishige Co., Ltd.. The 510(k) number is K003298.

When did MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR receive FDA 510(k) clearance?

MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR received FDA 510(k) clearance on 2000-11-21, under 510(k) number K003298.

Who is the listed applicant for MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR?

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 MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR?

The FDA product code for MO-202U THREE-AXIS JOYSTICK HYDRAULIC MICROMANIPULATOR 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.

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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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