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FDA 510(k)

Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves

K-Number: K203483 · 2021-02-01

ApplicantGuilin Hbm Health Protections, Inc.
Decision Date2021-02-01
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves is a medical device manufactured by Guilin Hbm Health Protections, Inc.. It received FDA 510(k) clearance on 2021-02-01 under approval number K203483. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves?

Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves is a medical device that received FDA 510(k) clearance on 2021-02-01. It is manufactured by Guilin Hbm Health Protections, Inc.. The 510(k) number is K203483.

When was Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves approved by the FDA?

Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves received FDA 510(k) clearance on 2021-02-01, under approval number K203483.

What company makes Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves?

Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves is manufactured by Guilin Hbm Health Protections, Inc..

What is the FDA product code for Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves?

The FDA product code for Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves is KGO.

Related Clinical Trials

NCT07559630 Rectal Arterial Embolization vs Band Ligation for the Treatment of Internal hemOrrhoidS RECRUITING NCT07372638 Sensorised Surgical Gloves for Neuroendovascular Procedures NOT_YET_RECRUITING

Other Devices by Guilin Hbm Health Protections, Inc.

K221748Medispo Rubber Surgical Gloves, Medispo Polyisoprene Surgical Gloves

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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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