DIFFERENTIAL CULTURE MED. MANNITOL SALT
K-Number: K841841 · 1984-05-25
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Device Summary
Frequently Asked Questions
What is the DIFFERENTIAL CULTURE MED. MANNITOL SALT?
DIFFERENTIAL CULTURE MED. MANNITOL SALT is a medical device that received FDA 510(k) clearance on 1984-05-25. The listed applicant is Microline Scientific. The 510(k) number is K841841.
When did DIFFERENTIAL CULTURE MED. MANNITOL SALT receive FDA 510(k) clearance?
DIFFERENTIAL CULTURE MED. MANNITOL SALT received FDA 510(k) clearance on 1984-05-25, under 510(k) number K841841.
Who is the listed applicant for DIFFERENTIAL CULTURE MED. MANNITOL SALT?
The FDA 510(k) record lists Microline Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIFFERENTIAL CULTURE MED. MANNITOL SALT?
The FDA product code for DIFFERENTIAL CULTURE MED. MANNITOL SALT 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 Microline Scientific 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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