CLOSTRIDIUM DIFFICILE MEDIA
K-Number: K831220 · 1983-05-09
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Device Summary
Frequently Asked Questions
What is the CLOSTRIDIUM DIFFICILE MEDIA?
CLOSTRIDIUM DIFFICILE MEDIA is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K831220.
When did CLOSTRIDIUM DIFFICILE MEDIA receive FDA 510(k) clearance?
CLOSTRIDIUM DIFFICILE MEDIA received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831220.
Who is the listed applicant for CLOSTRIDIUM DIFFICILE MEDIA?
The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLOSTRIDIUM DIFFICILE MEDIA?
The FDA product code for CLOSTRIDIUM DIFFICILE MEDIA is JSJ.
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 Gibco Laboratories Life Technologies, 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: JSJ)
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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