PLATELIA ASPERGILLUS EIA MODEL 62793
K-Number: K093678 · 2011-01-13
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Device Summary
Frequently Asked Questions
What is the PLATELIA ASPERGILLUS EIA MODEL 62793?
PLATELIA ASPERGILLUS EIA MODEL 62793 is a medical device that received FDA 510(k) clearance on 2011-01-13. The listed applicant is Bio-Rad. The 510(k) number is K093678.
When did PLATELIA ASPERGILLUS EIA MODEL 62793 receive FDA 510(k) clearance?
PLATELIA ASPERGILLUS EIA MODEL 62793 received FDA 510(k) clearance on 2011-01-13, under 510(k) number K093678.
Who is the listed applicant for PLATELIA ASPERGILLUS EIA MODEL 62793?
The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLATELIA ASPERGILLUS EIA MODEL 62793?
The FDA product code for PLATELIA ASPERGILLUS EIA MODEL 62793 is NOM.
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 Bio-Rad 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: NOM)
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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