MODIFIED SOYBEAN CASEIN DIGEST BROTH
K-Number: K831671 · 1983-07-28
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Device Summary
Frequently Asked Questions
What is the MODIFIED SOYBEAN CASEIN DIGEST BROTH?
MODIFIED SOYBEAN CASEIN DIGEST BROTH is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K831671.
When did MODIFIED SOYBEAN CASEIN DIGEST BROTH receive FDA 510(k) clearance?
MODIFIED SOYBEAN CASEIN DIGEST BROTH received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831671.
Who is the listed applicant for MODIFIED SOYBEAN CASEIN DIGEST BROTH?
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 MODIFIED SOYBEAN CASEIN DIGEST BROTH?
The FDA product code for MODIFIED SOYBEAN CASEIN DIGEST BROTH is JSG.
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: JSG)
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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