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FDA 510(k)

SUPER GLOVES PATIENT EXAM GLOVES (LATEX)

K-Number: K891856 · 1989-09-13

ApplicantWorld Wide Trade Network, Inc.
Decision Date1989-09-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUPER GLOVES PATIENT EXAM GLOVES (LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is World Wide Trade Network, Inc.. It received FDA 510(k) clearance on 1989-09-13 under 510(k) number K891856. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER GLOVES PATIENT EXAM GLOVES (LATEX)?

SUPER GLOVES PATIENT EXAM GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-09-13. The listed applicant is World Wide Trade Network, Inc.. The 510(k) number is K891856.

When did SUPER GLOVES PATIENT EXAM GLOVES (LATEX) receive FDA 510(k) clearance?

SUPER GLOVES PATIENT EXAM GLOVES (LATEX) received FDA 510(k) clearance on 1989-09-13, under 510(k) number K891856.

Who is the listed applicant for SUPER GLOVES PATIENT EXAM GLOVES (LATEX)?

The FDA 510(k) record lists World Wide Trade Network, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPER GLOVES PATIENT EXAM GLOVES (LATEX)?

The FDA product code for SUPER GLOVES PATIENT EXAM GLOVES (LATEX) is LYY.

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Related Devices (Code: LYY)

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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