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FDA 510(k)

LATEX EXAMINATION GLOVES, STYLE 510 LX

K-Number: K891420 · 1989-04-28

Decision Date1989-04-28
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES, STYLE 510 LX is the device name listed in this FDA 510(k) record. The listed applicant is C & K Mfg. & Sales Co.. It received FDA 510(k) clearance on 1989-04-28 under 510(k) number K891420. 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, STYLE 510 LX?

LATEX EXAMINATION GLOVES, STYLE 510 LX is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is C & K Mfg. & Sales Co.. The 510(k) number is K891420.

When did LATEX EXAMINATION GLOVES, STYLE 510 LX receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES, STYLE 510 LX received FDA 510(k) clearance on 1989-04-28, under 510(k) number K891420.

Who is the listed applicant for LATEX EXAMINATION GLOVES, STYLE 510 LX?

The FDA 510(k) record lists C & K Mfg. & Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAMINATION GLOVES, STYLE 510 LX?

The FDA product code for LATEX EXAMINATION GLOVES, STYLE 510 LX 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 C & K Mfg. & Sales Co. 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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