LAURYL TRYPTOSE BROTH
K-Number: K880126 · 1988-03-31
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Device Summary
Frequently Asked Questions
What is the LAURYL TRYPTOSE BROTH?
LAURYL TRYPTOSE BROTH is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Hardy Media. The 510(k) number is K880126.
When did LAURYL TRYPTOSE BROTH receive FDA 510(k) clearance?
LAURYL TRYPTOSE BROTH received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880126.
Who is the listed applicant for LAURYL TRYPTOSE BROTH?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAURYL TRYPTOSE BROTH?
The FDA product code for LAURYL TRYPTOSE BROTH is JSF.
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 Hardy Media 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: JSF)
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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