NEISSERIA MENINGITIDIS GR. A
K-Number: K840510 · 1984-03-23
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Device Summary
Frequently Asked Questions
What is the NEISSERIA MENINGITIDIS GR. A?
NEISSERIA MENINGITIDIS GR. A is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Scientific Device Laboratory, Inc.. The 510(k) number is K840510.
When did NEISSERIA MENINGITIDIS GR. A receive FDA 510(k) clearance?
NEISSERIA MENINGITIDIS GR. A received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840510.
Who is the listed applicant for NEISSERIA MENINGITIDIS GR. A?
The FDA 510(k) record lists Scientific Device Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEISSERIA MENINGITIDIS GR. A?
The FDA product code for NEISSERIA MENINGITIDIS GR. A is LSC.
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 Scientific Device Laboratory, 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: LSC)
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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