XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE
K-Number: K791787 · 1979-10-01
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Device Summary
Frequently Asked Questions
What is the XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE?
XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K791787.
When did XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE receive FDA 510(k) clearance?
XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791787.
Who is the listed applicant for XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE?
The FDA 510(k) record lists American Laboratory Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE?
The FDA product code for XYLOSE LYSINE DESOXYCHOLATE AGAR PLATE 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 American Laboratory Supply, 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: 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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