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FDA 510(k)

Grasping Forceps

K-Number: K152802 · 2016-01-21

ApplicantMicro-Tech (Nanjing) Co., Ltd.
Decision Date2016-01-21
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Grasping Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. It received FDA 510(k) clearance on 2016-01-21 under 510(k) number K152802. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Grasping Forceps?

Grasping Forceps is a medical device that received FDA 510(k) clearance on 2016-01-21. The listed applicant is Micro-Tech (Nanjing) Co., Ltd.. The 510(k) number is K152802.

When did Grasping Forceps receive FDA 510(k) clearance?

Grasping Forceps received FDA 510(k) clearance on 2016-01-21, under 510(k) number K152802.

Who is the listed applicant for Grasping Forceps?

The FDA 510(k) record lists Micro-Tech (Nanjing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Grasping Forceps?

The FDA product code for Grasping Forceps is OCZ.

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Related Devices (Code: OCZ)

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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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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