MIDDLEBROOK & COHN 7H11 AGAR BASE
K-Number: K834204 · 1984-01-03
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Device Summary
Frequently Asked Questions
What is the MIDDLEBROOK & COHN 7H11 AGAR BASE?
MIDDLEBROOK & COHN 7H11 AGAR BASE is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K834204.
When did MIDDLEBROOK & COHN 7H11 AGAR BASE receive FDA 510(k) clearance?
MIDDLEBROOK & COHN 7H11 AGAR BASE received FDA 510(k) clearance on 1984-01-03, under 510(k) number K834204.
Who is the listed applicant for MIDDLEBROOK & COHN 7H11 AGAR BASE?
The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIDDLEBROOK & COHN 7H11 AGAR BASE?
The FDA product code for MIDDLEBROOK & COHN 7H11 AGAR BASE is JSH.
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 Acumedia Manufacturers, 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: JSH)
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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