BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC
K-Number: K904232 · 1990-09-21
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Device Summary
Frequently Asked Questions
What is the BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC?
BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC is a medical device that received FDA 510(k) clearance on 1990-09-21. The listed applicant is Boston Medical Corp.. The 510(k) number is K904232.
When did BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC receive FDA 510(k) clearance?
BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC received FDA 510(k) clearance on 1990-09-21, under 510(k) number K904232.
Who is the listed applicant for BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC?
The FDA 510(k) record lists Boston Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC?
The FDA product code for BOSTON(R) BRAND LATEX EXAM GLOVES/HYPOALLERGENIC 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 Boston Medical 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.
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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