ELASTYREN POWDER-FREE SURGICAL GLOVE
K-Number: K971471 · 1998-02-09
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Device Summary
Frequently Asked Questions
What is the ELASTYREN POWDER-FREE SURGICAL GLOVE?
ELASTYREN POWDER-FREE SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 1998-02-09. The listed applicant is Eci Medical Technologies, Inc.. The 510(k) number is K971471.
When did ELASTYREN POWDER-FREE SURGICAL GLOVE receive FDA 510(k) clearance?
ELASTYREN POWDER-FREE SURGICAL GLOVE received FDA 510(k) clearance on 1998-02-09, under 510(k) number K971471.
Who is the listed applicant for ELASTYREN POWDER-FREE 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 ELASTYREN POWDER-FREE SURGICAL GLOVE?
The FDA product code for ELASTYREN POWDER-FREE SURGICAL GLOVE 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.
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.
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.
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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