BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE
K-Number: K850552 · 1985-03-11
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Device Summary
Frequently Asked Questions
What is the BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE?
BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Hardy Media. The 510(k) number is K850552.
When did BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE receive FDA 510(k) clearance?
BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850552.
Who is the listed applicant for BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE?
The FDA product code for BILE ESCULIN AGAR W/AZIDE, BEA W/AZIDE is JSI.
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 Hardy Media 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: JSI)
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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