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FDA 510(k)

CLINCARE LATEX SURGEON'S GLOVE

K-Number: K012067 · 2001-09-17

ApplicantTtk Healthcare , Ltd.
Decision Date2001-09-17
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLINCARE LATEX SURGEON'S GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Ttk Healthcare , Ltd.. It received FDA 510(k) clearance on 2001-09-17 under 510(k) number K012067. 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 CLINCARE LATEX SURGEON'S GLOVE?

CLINCARE LATEX SURGEON'S GLOVE is a medical device that received FDA 510(k) clearance on 2001-09-17. The listed applicant is Ttk Healthcare , Ltd.. The 510(k) number is K012067.

When did CLINCARE LATEX SURGEON'S GLOVE receive FDA 510(k) clearance?

CLINCARE LATEX SURGEON'S GLOVE received FDA 510(k) clearance on 2001-09-17, under 510(k) number K012067.

Who is the listed applicant for CLINCARE LATEX SURGEON'S GLOVE?

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

What is the FDA product code for CLINCARE LATEX SURGEON'S GLOVE?

The FDA product code for CLINCARE LATEX SURGEON'S GLOVE is KGO.

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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.

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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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