XYLOSE LYSINE DEOXYCHOLATE
K-Number: K832617 · 1983-09-12
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Device Summary
Frequently Asked Questions
What is the XYLOSE LYSINE DEOXYCHOLATE?
XYLOSE LYSINE DEOXYCHOLATE is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Carroll Biological Corp.. The 510(k) number is K832617.
When did XYLOSE LYSINE DEOXYCHOLATE receive FDA 510(k) clearance?
XYLOSE LYSINE DEOXYCHOLATE received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832617.
Who is the listed applicant for XYLOSE LYSINE DEOXYCHOLATE?
The FDA 510(k) record lists Carroll Biological Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XYLOSE LYSINE DEOXYCHOLATE?
The FDA product code for XYLOSE LYSINE DEOXYCHOLATE 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 Carroll Biological Corp. 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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