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FDA 510(k)

NEISSERIASTAT

K-Number: K860156 · 1986-03-11

ApplicantRichardson Scientific, Inc.
Decision Date1986-03-11
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NEISSERIASTAT is the device name listed in this FDA 510(k) record. The listed applicant is Richardson Scientific, Inc.. It received FDA 510(k) clearance on 1986-03-11 under 510(k) number K860156. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEISSERIASTAT?

NEISSERIASTAT is a medical device that received FDA 510(k) clearance on 1986-03-11. The listed applicant is Richardson Scientific, Inc.. The 510(k) number is K860156.

When did NEISSERIASTAT receive FDA 510(k) clearance?

NEISSERIASTAT received FDA 510(k) clearance on 1986-03-11, under 510(k) number K860156.

Who is the listed applicant for NEISSERIASTAT?

The FDA 510(k) record lists Richardson Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEISSERIASTAT?

The FDA product code for NEISSERIASTAT is JTO.

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Related Devices (Code: JTO)

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.

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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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