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FDA 510(k)

DEFEND LATEX EXAMINATION GLOVES

K-Number: K891257 · 1989-03-22

Decision Date1989-03-22
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DEFEND LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Carl Parker Associates, Inc.. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K891257. 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 DEFEND LATEX EXAMINATION GLOVES?

DEFEND LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Carl Parker Associates, Inc.. The 510(k) number is K891257.

When did DEFEND LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

DEFEND LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-03-22, under 510(k) number K891257.

Who is the listed applicant for DEFEND LATEX EXAMINATION GLOVES?

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

What is the FDA product code for DEFEND LATEX EXAMINATION GLOVES?

The FDA product code for DEFEND LATEX EXAMINATION 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 Carl Parker Associates, 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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