CAMPYLOCACTER SELECTIVE AGAR BLASER'S
K-Number: K830076 · 1983-02-09
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Device Summary
Frequently Asked Questions
What is the CAMPYLOCACTER SELECTIVE AGAR BLASER'S?
CAMPYLOCACTER SELECTIVE AGAR BLASER'S is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is bioMerieux, Inc.. The 510(k) number is K830076.
When did CAMPYLOCACTER SELECTIVE AGAR BLASER'S receive FDA 510(k) clearance?
CAMPYLOCACTER SELECTIVE AGAR BLASER'S received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830076.
Who is the listed applicant for CAMPYLOCACTER SELECTIVE AGAR BLASER'S?
The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAMPYLOCACTER SELECTIVE AGAR BLASER'S?
The FDA product code for CAMPYLOCACTER SELECTIVE AGAR BLASER'S 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 bioMerieux, 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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