LEVINE EOSIN METHYLENE BLUE AGAR
K-Number: K841751 · 1984-05-31
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Device Summary
Frequently Asked Questions
What is the LEVINE EOSIN METHYLENE BLUE AGAR?
LEVINE EOSIN METHYLENE BLUE AGAR is a medical device that received FDA 510(k) clearance on 1984-05-31. The listed applicant is The Montana Deaconess Medical Center. The 510(k) number is K841751.
When did LEVINE EOSIN METHYLENE BLUE AGAR receive FDA 510(k) clearance?
LEVINE EOSIN METHYLENE BLUE AGAR received FDA 510(k) clearance on 1984-05-31, under 510(k) number K841751.
Who is the listed applicant for LEVINE EOSIN METHYLENE BLUE AGAR?
The FDA 510(k) record lists The Montana Deaconess Medical Center as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEVINE EOSIN METHYLENE BLUE AGAR?
The FDA product code for LEVINE EOSIN METHYLENE BLUE 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 The Montana Deaconess Medical Center 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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