EILE-ESCULIN AZIDE AGAR
K-Number: K841132 · 1984-03-23
Advertisement
Device Summary
Frequently Asked Questions
What is the EILE-ESCULIN AZIDE AGAR?
EILE-ESCULIN AZIDE AGAR is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Anaerobe Systems. The 510(k) number is K841132.
When did EILE-ESCULIN AZIDE AGAR receive FDA 510(k) clearance?
EILE-ESCULIN AZIDE AGAR received FDA 510(k) clearance on 1984-03-23, under 510(k) number K841132.
Who is the listed applicant for EILE-ESCULIN AZIDE AGAR?
The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EILE-ESCULIN AZIDE AGAR?
The FDA product code for EILE-ESCULIN AZIDE AGAR 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 Anaerobe Systems 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.
Advertisement