FASTIDIOUS INOCULUM BROTH
K-Number: K883075 · 1988-08-15
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Device Summary
Frequently Asked Questions
What is the FASTIDIOUS INOCULUM BROTH?
FASTIDIOUS INOCULUM BROTH is a medical device that received FDA 510(k) clearance on 1988-08-15. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K883075.
When did FASTIDIOUS INOCULUM BROTH receive FDA 510(k) clearance?
FASTIDIOUS INOCULUM BROTH received FDA 510(k) clearance on 1988-08-15, under 510(k) number K883075.
Who is the listed applicant for FASTIDIOUS INOCULUM BROTH?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FASTIDIOUS INOCULUM BROTH?
The FDA product code for FASTIDIOUS INOCULUM BROTH is JSD.
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 Baxter Healthcare Corp 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: JSD)
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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