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FDA 510(k)

CAMPYLOCACTER SELECTIVE AGAR BLASER'S

K-Number: K830076 · 1983-02-09

Decision Date1983-02-09
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPYLOCACTER SELECTIVE AGAR BLASER'S is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1983-02-09 under 510(k) number K830076. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 248 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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