MANNITOL SALT AGAR (MSA) PRODUCT #P1706
K-Number: K873227 · 1987-09-23
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Device Summary
Frequently Asked Questions
What is the MANNITOL SALT AGAR (MSA) PRODUCT #P1706?
MANNITOL SALT AGAR (MSA) PRODUCT #P1706 is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is Lakewood Biochemical Co., Inc.. The 510(k) number is K873227.
When did MANNITOL SALT AGAR (MSA) PRODUCT #P1706 receive FDA 510(k) clearance?
MANNITOL SALT AGAR (MSA) PRODUCT #P1706 received FDA 510(k) clearance on 1987-09-23, under 510(k) number K873227.
Who is the listed applicant for MANNITOL SALT AGAR (MSA) PRODUCT #P1706?
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 MANNITOL SALT AGAR (MSA) PRODUCT #P1706?
The FDA product code for MANNITOL SALT AGAR (MSA) PRODUCT #P1706 is JSI.
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: JSI)
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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