SABOURAUD AGAR MODIFIED
K-Number: K791670 · 1979-10-01
Advertisement
Device Summary
Frequently Asked Questions
What is the SABOURAUD AGAR MODIFIED?
SABOURAUD AGAR MODIFIED is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K791670.
When did SABOURAUD AGAR MODIFIED receive FDA 510(k) clearance?
SABOURAUD AGAR MODIFIED received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791670.
Who is the listed applicant for SABOURAUD AGAR MODIFIED?
The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SABOURAUD AGAR MODIFIED?
The FDA product code for SABOURAUD AGAR MODIFIED 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 Isle Media and Sterile Products, 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.
Advertisement