TRYPTICASE SOY BROTH TUBE
K-Number: K840075 · 1984-02-03
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Device Summary
Frequently Asked Questions
What is the TRYPTICASE SOY BROTH TUBE?
TRYPTICASE SOY BROTH TUBE is a medical device that received FDA 510(k) clearance on 1984-02-03. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K840075.
When did TRYPTICASE SOY BROTH TUBE receive FDA 510(k) clearance?
TRYPTICASE SOY BROTH TUBE received FDA 510(k) clearance on 1984-02-03, under 510(k) number K840075.
Who is the listed applicant for TRYPTICASE SOY BROTH TUBE?
The FDA 510(k) record lists Otisville Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRYPTICASE SOY BROTH TUBE?
The FDA product code for TRYPTICASE SOY BROTH TUBE 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 Otisville Biotech, 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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