POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421
K-Number: K882463 · 1988-06-22
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Device Summary
Frequently Asked Questions
What is the POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421?
POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421 is a medical device that received FDA 510(k) clearance on 1988-06-22. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K882463.
When did POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421 receive FDA 510(k) clearance?
POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421 received FDA 510(k) clearance on 1988-06-22, under 510(k) number K882463.
Who is the listed applicant for POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421?
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 POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421?
The FDA product code for POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421 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 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: 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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