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FDA 510(k)

ARISTA AND ORIENT SURGICAL GLOVES

K-Number: K884633 · 1989-04-20

ApplicantDurante Intl., Inc.
Decision Date1989-04-20
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARISTA AND ORIENT SURGICAL GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Durante Intl., Inc.. It received FDA 510(k) clearance on 1989-04-20 under 510(k) number K884633. 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 ARISTA AND ORIENT SURGICAL GLOVES?

ARISTA AND ORIENT SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-20. The listed applicant is Durante Intl., Inc.. The 510(k) number is K884633.

When did ARISTA AND ORIENT SURGICAL GLOVES receive FDA 510(k) clearance?

ARISTA AND ORIENT SURGICAL GLOVES received FDA 510(k) clearance on 1989-04-20, under 510(k) number K884633.

Who is the listed applicant for ARISTA AND ORIENT SURGICAL GLOVES?

The FDA 510(k) record lists Durante Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARISTA AND ORIENT SURGICAL GLOVES?

The FDA product code for ARISTA AND ORIENT SURGICAL GLOVES is KGO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Durante Intl., Inc. 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.

K891677COATED ISOLATION GOWN

Related Devices (Code: KGO)

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.

K260558Latex Powder Free Surgical Gloves Tested for Use with Chemotherapy Drugs and Fentanyl Citrate; Latex Powder Free Surgical Gloves with Colloidal Oatmeal Tested for Use with Chemotherapy Drugs and Fentanyl CitrateHartalega NGC Sdn. Bhd.K253060Sterile Latex Powder Free Surgical GlovesProtect Gloves Company LimitedK250313Sterile Powder Free Synthetic Rubber Surgeon’s Gloves, Green Color, Tested For Use With Chemotherapy Drugs and Gastric AcidHarps Europe Manufacturing GmbHK240790Polyisoprene Surgical glovesSuzhou Colour-Way New Material Co., Ltd.K232079Natural Rubber Latex Surgical Glove, Powder Free, Sterile, Tested for Use with Chemotherapy Drugs and Fentanyl (Green); Natural Rubber Latex (Strip&Coat)/(Strip&Pack) Surgical Glove, Powder Free, Sterile, Tested for Use with Chemotherapy Drugs and FentanylWrp Asia Pacific Sdn. Bhd.K232444Sterile Powder Free Latex Surgical Gloves, Tested for Use with Chemotherapy DrugsGrand Work Plastic Products Co., Ltd.

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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