MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181
K-Number: K882351 · 1988-06-28
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181?
MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181 is a medical device that received FDA 510(k) clearance on 1988-06-28. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K882351.
When did MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181 receive FDA 510(k) clearance?
MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181 received FDA 510(k) clearance on 1988-06-28, under 510(k) number K882351.
Who is the listed applicant for MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181?
The FDA 510(k) record lists Lakewood Biochemical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181?
The FDA product code for MUELLER HINTON AGAR PLATES P3318/1&2/P3418/P34181 is JTZ.
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 Lakewood Biochemical Co., 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: JTZ)
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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