SABOURAUD DEXTROSE AGAR
K-Number: K864250 · 1987-03-31
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Device Summary
Frequently Asked Questions
What is the SABOURAUD DEXTROSE AGAR?
SABOURAUD DEXTROSE AGAR is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864250.
When did SABOURAUD DEXTROSE AGAR receive FDA 510(k) clearance?
SABOURAUD DEXTROSE AGAR received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864250.
Who is the listed applicant for SABOURAUD DEXTROSE AGAR?
The FDA 510(k) record lists Mds Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SABOURAUD DEXTROSE AGAR?
The FDA product code for SABOURAUD DEXTROSE AGAR 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 Mds Laboratories, 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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