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FDA 510(k)

BOSTON MEDICAL LATEX EXAM GLOVES

K-Number: K952695 · 1995-08-11

Decision Date1995-08-11
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOSTON MEDICAL LATEX EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shun Thai Rubber Gloves Industry Co., Ltd.. It received FDA 510(k) clearance on 1995-08-11 under 510(k) number K952695. 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 BOSTON MEDICAL LATEX EXAM GLOVES?

BOSTON MEDICAL LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1995-08-11. The listed applicant is Shun Thai Rubber Gloves Industry Co., Ltd.. The 510(k) number is K952695.

When did BOSTON MEDICAL LATEX EXAM GLOVES receive FDA 510(k) clearance?

BOSTON MEDICAL LATEX EXAM GLOVES received FDA 510(k) clearance on 1995-08-11, under 510(k) number K952695.

Who is the listed applicant for BOSTON MEDICAL LATEX EXAM GLOVES?

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

What is the FDA product code for BOSTON MEDICAL LATEX EXAM GLOVES?

The FDA product code for BOSTON MEDICAL LATEX EXAM GLOVES 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 Shun Thai Rubber Gloves Industry Co., Ltd. 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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