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FDA 510(k)

VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.)

K-Number: K893098 · 1989-06-14

ApplicantJason Co.
Decision Date1989-06-14
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.) is the device name listed in this FDA 510(k) record. The listed applicant is Jason Co.. It received FDA 510(k) clearance on 1989-06-14 under 510(k) number K893098. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.)?

VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.) is a medical device that received FDA 510(k) clearance on 1989-06-14. The listed applicant is Jason Co.. The 510(k) number is K893098.

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

VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.) received FDA 510(k) clearance on 1989-06-14, under 510(k) number K893098.

Who is the listed applicant for VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.)?

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

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

The FDA product code for VINYL EXAM GLOVES (MFG. TOPLAS INDUSTRIAL CO.) is LYZ.

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Related Devices (Code: LYZ)

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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