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FDA 510(k)

KULTSURE (CULTURE TRANSPORT)

K-Number: K860178 · 1986-04-04

ApplicantNcs Diagnostics, Inc.
Decision Date1986-04-04
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

KULTSURE (CULTURE TRANSPORT) is the device name listed in this FDA 510(k) record. The listed applicant is Ncs Diagnostics, Inc.. It received FDA 510(k) clearance on 1986-04-04 under 510(k) number K860178. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KULTSURE (CULTURE TRANSPORT)?

KULTSURE (CULTURE TRANSPORT) is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Ncs Diagnostics, Inc.. The 510(k) number is K860178.

When did KULTSURE (CULTURE TRANSPORT) receive FDA 510(k) clearance?

KULTSURE (CULTURE TRANSPORT) received FDA 510(k) clearance on 1986-04-04, under 510(k) number K860178.

Who is the listed applicant for KULTSURE (CULTURE TRANSPORT)?

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

What is the FDA product code for KULTSURE (CULTURE TRANSPORT)?

The FDA product code for KULTSURE (CULTURE TRANSPORT) is JSM.

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Other records listing Ncs Diagnostics, 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.

K943499KULTSURE STARSWAB(M240), MODIFICATIONK943498KULTSURE STARSWAB (M210), MODIFICATIONK882811STREPSLIDEK881209ASO SLIDE TESTK874019STAPHSLIDEK871404KULTSURE

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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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