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FDA 510(k)

PROSON PATIENT EXAMINATION GLOVES

K-Number: K893076 · 1989-07-31

ApplicantLong Far Industry Co., Ltd.
Decision Date1989-07-31
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROSON PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Long Far Industry Co., Ltd.. It received FDA 510(k) clearance on 1989-07-31 under 510(k) number K893076. 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 PROSON PATIENT EXAMINATION GLOVES?

PROSON PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-07-31. The listed applicant is Long Far Industry Co., Ltd.. The 510(k) number is K893076.

When did PROSON PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

PROSON PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-07-31, under 510(k) number K893076.

Who is the listed applicant for PROSON PATIENT EXAMINATION GLOVES?

The FDA 510(k) record lists Long Far Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROSON PATIENT EXAMINATION GLOVES?

The FDA product code for PROSON PATIENT EXAMINATION GLOVES 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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