IAFP BRAIN HEART INFUSION BROTH
K-Number: K872667 · 1987-08-07
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Device Summary
Frequently Asked Questions
What is the IAFP BRAIN HEART INFUSION BROTH?
IAFP BRAIN HEART INFUSION BROTH is a medical device that received FDA 510(k) clearance on 1987-08-07. The listed applicant is I.A.F. Production, Inc.. The 510(k) number is K872667.
When did IAFP BRAIN HEART INFUSION BROTH receive FDA 510(k) clearance?
IAFP BRAIN HEART INFUSION BROTH received FDA 510(k) clearance on 1987-08-07, under 510(k) number K872667.
Who is the listed applicant for IAFP BRAIN HEART INFUSION BROTH?
The FDA 510(k) record lists I.A.F. Production, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IAFP BRAIN HEART INFUSION BROTH?
The FDA product code for IAFP BRAIN HEART INFUSION 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 I.A.F. Production, 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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