IAFP CAMPYLOBACTER BLASER
K-Number: K872684 · 1987-08-11
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Device Summary
Frequently Asked Questions
What is the IAFP CAMPYLOBACTER BLASER?
IAFP CAMPYLOBACTER BLASER is a medical device that received FDA 510(k) clearance on 1987-08-11. The listed applicant is I.A.F. Production, Inc.. The 510(k) number is K872684.
When did IAFP CAMPYLOBACTER BLASER receive FDA 510(k) clearance?
IAFP CAMPYLOBACTER BLASER received FDA 510(k) clearance on 1987-08-11, under 510(k) number K872684.
Who is the listed applicant for IAFP CAMPYLOBACTER BLASER?
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 CAMPYLOBACTER BLASER?
The FDA product code for IAFP CAMPYLOBACTER BLASER is JSJ.
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: JSJ)
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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