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FDA 510(k)

IM-11 PNEUMATIC MICROINJECTOR

K-Number: K113712 · 2012-03-15

Decision Date2012-03-15
Product CodeMQJ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

IM-11 PNEUMATIC MICROINJECTOR 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 2012-03-15 under 510(k) number K113712. 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 IM-11 PNEUMATIC MICROINJECTOR?

IM-11 PNEUMATIC MICROINJECTOR is a medical device that received FDA 510(k) clearance on 2012-03-15. The listed applicant is Narishige Co., Ltd.. The 510(k) number is K113712.

When did IM-11 PNEUMATIC MICROINJECTOR receive FDA 510(k) clearance?

IM-11 PNEUMATIC MICROINJECTOR received FDA 510(k) clearance on 2012-03-15, under 510(k) number K113712.

Who is the listed applicant for IM-11 PNEUMATIC MICROINJECTOR?

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 IM-11 PNEUMATIC MICROINJECTOR?

The FDA product code for IM-11 PNEUMATIC MICROINJECTOR 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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