APL XYLOSE LYSINE DEOXYCHOLATE AGAR
K-Number: K853611 · 1985-09-12
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Device Summary
Frequently Asked Questions
What is the APL XYLOSE LYSINE DEOXYCHOLATE AGAR?
APL XYLOSE LYSINE DEOXYCHOLATE AGAR is a medical device that received FDA 510(k) clearance on 1985-09-12. The listed applicant is Apl Medical Supplies. The 510(k) number is K853611.
When did APL XYLOSE LYSINE DEOXYCHOLATE AGAR receive FDA 510(k) clearance?
APL XYLOSE LYSINE DEOXYCHOLATE AGAR received FDA 510(k) clearance on 1985-09-12, under 510(k) number K853611.
Who is the listed applicant for APL XYLOSE LYSINE DEOXYCHOLATE AGAR?
The FDA 510(k) record lists Apl Medical Supplies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APL XYLOSE LYSINE DEOXYCHOLATE AGAR?
The FDA product code for APL XYLOSE LYSINE DEOXYCHOLATE AGAR 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 Apl Medical Supplies 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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