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FDA 510(k)

POWDER FREE SURGEONS GLOVE

K-Number: K982586 · 1998-08-11

Decision Date1998-08-11
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWDER FREE SURGEONS GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Shiva Medicare , Ltd.. It received FDA 510(k) clearance on 1998-08-11 under 510(k) number K982586. 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 POWDER FREE SURGEONS GLOVE?

POWDER FREE SURGEONS GLOVE is a medical device that received FDA 510(k) clearance on 1998-08-11. The listed applicant is Shiva Medicare , Ltd.. The 510(k) number is K982586.

When did POWDER FREE SURGEONS GLOVE receive FDA 510(k) clearance?

POWDER FREE SURGEONS GLOVE received FDA 510(k) clearance on 1998-08-11, under 510(k) number K982586.

Who is the listed applicant for POWDER FREE SURGEONS GLOVE?

The FDA 510(k) record lists Shiva Medicare , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER FREE SURGEONS GLOVE?

The FDA product code for POWDER FREE SURGEONS 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 Shiva Medicare , 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: 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

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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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