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FDA 510(k)

NEISSERIA MENINGITIDIS GR. B

K-Number: K840509 · 1984-03-23

Decision Date1984-03-23
Product CodeLSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NEISSERIA MENINGITIDIS GR. B is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Device Laboratory, Inc.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840509. The device is classified under product code LSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEISSERIA MENINGITIDIS GR. B?

NEISSERIA MENINGITIDIS GR. B 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 K840509.

When did NEISSERIA MENINGITIDIS GR. B receive FDA 510(k) clearance?

NEISSERIA MENINGITIDIS GR. B received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840509.

Who is the listed applicant for NEISSERIA MENINGITIDIS GR. B?

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. B?

The FDA product code for NEISSERIA MENINGITIDIS GR. B 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.

View all 28 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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