Rescue Pulmonary Grasping Forceps
K-Number: K202987 · 2021-04-29
Device Summary
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. The listed applicant is Anrei Medical (Hangzhou) Co., Ltd.. The 510(k) number is K202987.
When did Rescue Pulmonary Grasping Forceps receive FDA 510(k) clearance?
Rescue Pulmonary Grasping Forceps received FDA 510(k) clearance on 2021-04-29, under 510(k) number K202987.
Who is the listed applicant for Rescue Pulmonary Grasping Forceps?
The FDA 510(k) record lists Anrei Medical (Hangzhou) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Rescue Pulmonary Grasping Forceps?
The FDA product code for Rescue Pulmonary Grasping Forceps is EOQ.
Other records listing Anrei Medical (Hangzhou) 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: EOQ)
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.