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FDA 510(k)

PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.)

K-Number: K892100 · 1989-05-08

Decision Date1989-05-08
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.) is the device name listed in this FDA 510(k) record. The listed applicant is Ergo Intl., Ent., Inc.. It received FDA 510(k) clearance on 1989-05-08 under 510(k) number K892100. 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. SHUN JUN TRADING CO.)?

PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.) is a medical device that received FDA 510(k) clearance on 1989-05-08. The listed applicant is Ergo Intl., Ent., Inc.. The 510(k) number is K892100.

When did PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.) received FDA 510(k) clearance on 1989-05-08, under 510(k) number K892100.

Who is the listed applicant for PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.)?

The FDA 510(k) record lists Ergo Intl., Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.)?

The FDA product code for PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.) is LYY.

Related Clinical Trials

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.

Other records listing Ergo Intl., Ent., Inc. as applicant

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.

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.

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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