M. CAT. BUTYRATE DISC
K-Number: K905666 · 1991-02-26
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Device Summary
Frequently Asked Questions
What is the M. CAT. BUTYRATE DISC?
M. CAT. BUTYRATE DISC is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K905666.
When did M. CAT. BUTYRATE DISC receive FDA 510(k) clearance?
M. CAT. BUTYRATE DISC received FDA 510(k) clearance on 1991-02-26, under 510(k) number K905666.
Who is the listed applicant for M. CAT. BUTYRATE DISC?
The FDA 510(k) record lists Carr-Scarborough Microbiologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M. CAT. BUTYRATE DISC?
The FDA product code for M. CAT. BUTYRATE DISC is JTO.
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 Carr-Scarborough Microbiologicals, 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: JTO)
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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