DC AGAR (DESOXYCHOLATE CITRATE AGAR)
K-Number: K791816 · 1979-10-01
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Device Summary
Frequently Asked Questions
What is the DC AGAR (DESOXYCHOLATE CITRATE AGAR)?
DC AGAR (DESOXYCHOLATE CITRATE AGAR) 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 K791816.
When did DC AGAR (DESOXYCHOLATE CITRATE AGAR) receive FDA 510(k) clearance?
DC AGAR (DESOXYCHOLATE CITRATE AGAR) received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791816.
Who is the listed applicant for DC AGAR (DESOXYCHOLATE CITRATE AGAR)?
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 DC AGAR (DESOXYCHOLATE CITRATE AGAR)?
The FDA product code for DC AGAR (DESOXYCHOLATE CITRATE 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 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: 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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