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FDA 510(k)

ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE

K-Number: K021598 · 2002-06-10

ApplicantEci Medical Technologies, Inc.
Decision Date2002-06-10
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Eci Medical Technologies, Inc.. It received FDA 510(k) clearance on 2002-06-10 under 510(k) number K021598. 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 ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE?

ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 2002-06-10. The listed applicant is Eci Medical Technologies, Inc.. The 510(k) number is K021598.

When did ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE receive FDA 510(k) clearance?

ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE received FDA 510(k) clearance on 2002-06-10, under 510(k) number K021598.

Who is the listed applicant for ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE?

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

What is the FDA product code for ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE?

The FDA product code for ELASTYLITE SYNTHETIC POWDERED SURGICAL GLOVE is KGO.

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Other records listing Eci Medical Technologies, 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.

K020918ELASTYFREE SYNTHETIC POWDER-FREE SURGICAL GLOVEK984337ELASTYLON POWDER-FREE SURGICAL GLOVEK971471ELASTYREN POWDER-FREE SURGICAL GLOVEK970015ELASTYREN POWDER-FREE PATIENT EXAMINATION GLOVESK954533ELASTYREN HYPOALLERGENIC PATIENT EXAMINATION GLOVESK954535ELASTYREN HYPOALLERGENIC SURGICAL GLOVES

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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

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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