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FDA 510(k)

Rescue Pulmonary Grasping Forceps

K-Number: K202987 · 2021-04-29

ApplicantAnrei Medical (Hangzhou) Co., Ltd.
Decision Date2021-04-29
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Rescue Pulmonary Grasping Forceps is a medical device manufactured by Anrei Medical (Hangzhou) Co., Ltd.. It received FDA 510(k) clearance on 2021-04-29 under approval number K202987. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Rescue Pulmonary Grasping Forceps?

Rescue Pulmonary Grasping Forceps is a medical device that received FDA 510(k) clearance on 2021-04-29. It is manufactured by Anrei Medical (Hangzhou) Co., Ltd.. The 510(k) number is K202987.

When was Rescue Pulmonary Grasping Forceps approved by the FDA?

Rescue Pulmonary Grasping Forceps received FDA 510(k) clearance on 2021-04-29, under approval number K202987.

What company makes Rescue Pulmonary Grasping Forceps?

Rescue Pulmonary Grasping Forceps is manufactured by Anrei Medical (Hangzhou) Co., Ltd..

What is the FDA product code for Rescue Pulmonary Grasping Forceps?

The FDA product code for Rescue Pulmonary Grasping Forceps is EOQ.

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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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