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FDA 510(k)

PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY)

K-Number: K905585 · 1990-12-21

ApplicantPioneer Trading Co.
Decision Date1990-12-21
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY) is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Trading Co.. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K905585. 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: LIAONING MACHINERY)?

PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY) is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Pioneer Trading Co.. The 510(k) number is K905585.

When did PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY) received FDA 510(k) clearance on 1990-12-21, under 510(k) number K905585.

Who is the listed applicant for PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY)?

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

What is the FDA product code for PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY)?

The FDA product code for PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY) 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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