BIOTIS (TM) STARCH HYDROLYSIS WITH BCP
K-Number: K874174 · 1987-12-04
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Device Summary
Frequently Asked Questions
What is the BIOTIS (TM) STARCH HYDROLYSIS WITH BCP?
BIOTIS (TM) STARCH HYDROLYSIS WITH BCP is a medical device that received FDA 510(k) clearance on 1987-12-04. The listed applicant is Otisville Biopharm, Inc.. The 510(k) number is K874174.
When did BIOTIS (TM) STARCH HYDROLYSIS WITH BCP receive FDA 510(k) clearance?
BIOTIS (TM) STARCH HYDROLYSIS WITH BCP received FDA 510(k) clearance on 1987-12-04, under 510(k) number K874174.
Who is the listed applicant for BIOTIS (TM) STARCH HYDROLYSIS WITH BCP?
The FDA 510(k) record lists Otisville Biopharm, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOTIS (TM) STARCH HYDROLYSIS WITH BCP?
The FDA product code for BIOTIS (TM) STARCH HYDROLYSIS WITH BCP 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 Otisville Biopharm, 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: 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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