PROASIA, MODEL L4501
K-Number: K052486 · 2005-10-07
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Device Summary
Frequently Asked Questions
What is the PROASIA, MODEL L4501?
PROASIA, MODEL L4501 is a medical device that received FDA 510(k) clearance on 2005-10-07. The listed applicant is Proasia Limited. The 510(k) number is K052486.
When did PROASIA, MODEL L4501 receive FDA 510(k) clearance?
PROASIA, MODEL L4501 received FDA 510(k) clearance on 2005-10-07, under 510(k) number K052486.
Who is the listed applicant for PROASIA, MODEL L4501?
The FDA 510(k) record lists Proasia Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROASIA, MODEL L4501?
The FDA product code for PROASIA, MODEL L4501 is INI.
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 Proasia Limited 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: INI)
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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