MIDDLEBROOK 7H10 AGAR
K-Number: K870646 · 1987-04-14
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Device Summary
Frequently Asked Questions
What is the MIDDLEBROOK 7H10 AGAR?
MIDDLEBROOK 7H10 AGAR is a medical device that received FDA 510(k) clearance on 1987-04-14. The listed applicant is Hardy Media. The 510(k) number is K870646.
When did MIDDLEBROOK 7H10 AGAR receive FDA 510(k) clearance?
MIDDLEBROOK 7H10 AGAR received FDA 510(k) clearance on 1987-04-14, under 510(k) number K870646.
Who is the listed applicant for MIDDLEBROOK 7H10 AGAR?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIDDLEBROOK 7H10 AGAR?
The FDA product code for MIDDLEBROOK 7H10 AGAR is KZI.
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 Hardy Media 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: KZI)
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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