MIDDLEBROOK 7H11 AGAR (PLATE)
K-Number: K771661 · 1977-09-12
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Device Summary
Frequently Asked Questions
What is the MIDDLEBROOK 7H11 AGAR (PLATE)?
MIDDLEBROOK 7H11 AGAR (PLATE) is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K771661.
When did MIDDLEBROOK 7H11 AGAR (PLATE) receive FDA 510(k) clearance?
MIDDLEBROOK 7H11 AGAR (PLATE) received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771661.
Who is the listed applicant for MIDDLEBROOK 7H11 AGAR (PLATE)?
The FDA 510(k) record lists Granite Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIDDLEBROOK 7H11 AGAR (PLATE)?
The FDA product code for MIDDLEBROOK 7H11 AGAR (PLATE) 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 Granite Diagnostics, 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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