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FDA 510(k)

PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.)

K-Number: K892686 · 1989-05-25

ApplicantIntl. Visco Group
Decision Date1989-05-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.) is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Visco Group. It received FDA 510(k) clearance on 1989-05-25 under 510(k) number K892686. 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 PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.)?

PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.) is a medical device that received FDA 510(k) clearance on 1989-05-25. The listed applicant is Intl. Visco Group. The 510(k) number is K892686.

When did PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.) received FDA 510(k) clearance on 1989-05-25, under 510(k) number K892686.

Who is the listed applicant for PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.)?

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

What is the FDA product code for PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.)?

The FDA product code for PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.) 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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