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FDA 510(k)

MIC NON-STERILE LATEX GLOVES

K-Number: K891160 · 1989-10-13

Decision Date1989-10-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MIC NON-STERILE LATEX GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Asia Dynamics, Inc.. It received FDA 510(k) clearance on 1989-10-13 under 510(k) number K891160. 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 MIC NON-STERILE LATEX GLOVES?

MIC NON-STERILE LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Asia Dynamics, Inc.. The 510(k) number is K891160.

When did MIC NON-STERILE LATEX GLOVES receive FDA 510(k) clearance?

MIC NON-STERILE LATEX GLOVES received FDA 510(k) clearance on 1989-10-13, under 510(k) number K891160.

Who is the listed applicant for MIC NON-STERILE LATEX GLOVES?

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

What is the FDA product code for MIC NON-STERILE LATEX GLOVES?

The FDA product code for MIC NON-STERILE LATEX 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 Asia Dynamics, 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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