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FDA 510(k)

LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX)

K-Number: K893351 · 1989-11-17

Decision Date1989-11-17
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is China National Medicines & Health Prod. I/E Corp.. It received FDA 510(k) clearance on 1989-11-17 under 510(k) number K893351. 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 LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX)?

LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX) is a medical device that received FDA 510(k) clearance on 1989-11-17. The listed applicant is China National Medicines & Health Prod. I/E Corp.. The 510(k) number is K893351.

When did LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX) receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX) received FDA 510(k) clearance on 1989-11-17, under 510(k) number K893351.

Who is the listed applicant for LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX)?

The FDA 510(k) record lists China National Medicines & Health Prod. I/E Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX)?

The FDA product code for LATEX EXAMINATION GLOVES (MFG. ANHUI BENGBU LATEX) 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 China National Medicines & Health Prod. I/E Corp. 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 12 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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