LATEX EXAMINATION GLOVES, STYLE 510 LX
K-Number: K891420 · 1989-04-28
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Device Summary
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
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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