GLOVCO EBONY
K-Number: K013828 · 2002-08-13
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Device Summary
Frequently Asked Questions
What is the GLOVCO EBONY?
GLOVCO EBONY is a medical device that received FDA 510(k) clearance on 2002-08-13. The listed applicant is Glovco (M) Sdn. Bhd.. The 510(k) number is K013828.
When did GLOVCO EBONY receive FDA 510(k) clearance?
GLOVCO EBONY received FDA 510(k) clearance on 2002-08-13, under 510(k) number K013828.
Who is the listed applicant for GLOVCO EBONY?
The FDA 510(k) record lists Glovco (M) Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLOVCO EBONY?
The FDA product code for GLOVCO EBONY 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 Glovco (M) Sdn. Bhd. 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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