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FDA 510(k)

ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE

K-Number: K973461 · 1997-12-09

ApplicantAnsell Perry
Decision Date1997-12-09
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Ansell Perry. It received FDA 510(k) clearance on 1997-12-09 under 510(k) number K973461. 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 ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE?

ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 1997-12-09. The listed applicant is Ansell Perry. The 510(k) number is K973461.

When did ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE receive FDA 510(k) clearance?

ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE received FDA 510(k) clearance on 1997-12-09, under 510(k) number K973461.

Who is the listed applicant for ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE?

The FDA 510(k) record lists Ansell Perry as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE?

The FDA product code for ELITE POWDER FREE POLYURETHANE SYNTHETIC SURGICAL GLOVE is KGO.

Related Clinical Trials

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Other records listing Ansell Perry 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.

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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.

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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