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FDA 510(k)

PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY

K-Number: K891739 · 1989-04-14

Decision Date1989-04-14
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY is the device name listed in this FDA 510(k) record. The listed applicant is Brilliant Ray Intl., Inc.. It received FDA 510(k) clearance on 1989-04-14 under 510(k) number K891739. 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 GLOVE (LATEX) MFG. TIANJIN JI COUNTY?

PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY is a medical device that received FDA 510(k) clearance on 1989-04-14. The listed applicant is Brilliant Ray Intl., Inc.. The 510(k) number is K891739.

When did PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY receive FDA 510(k) clearance?

PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY received FDA 510(k) clearance on 1989-04-14, under 510(k) number K891739.

Who is the listed applicant for PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY?

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

What is the FDA product code for PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY?

The FDA product code for PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY 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 Brilliant Ray Intl., 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.

View all 7 devices →

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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