JBAIDS ANTHRAC DETECTION SYSTEM
K-Number: K051713 · 2005-11-18
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Device Summary
Frequently Asked Questions
What is the JBAIDS ANTHRAC DETECTION SYSTEM?
JBAIDS ANTHRAC DETECTION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-11-18. The listed applicant is Idaho Technology, Inc.. The 510(k) number is K051713.
When did JBAIDS ANTHRAC DETECTION SYSTEM receive FDA 510(k) clearance?
JBAIDS ANTHRAC DETECTION SYSTEM received FDA 510(k) clearance on 2005-11-18, under 510(k) number K051713.
Who is the listed applicant for JBAIDS ANTHRAC DETECTION SYSTEM?
The FDA 510(k) record lists Idaho Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JBAIDS ANTHRAC DETECTION SYSTEM?
The FDA product code for JBAIDS ANTHRAC DETECTION SYSTEM is NHT.
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 Idaho Technology, Inc. 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: NHT)
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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