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FDA 510(k)

STAPHSLIDE

K-Number: K874019 · 1987-10-28

ApplicantNcs Diagnostics, Inc.
Decision Date1987-10-28
Product CodeJWX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

STAPHSLIDE 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 1987-10-28 under 510(k) number K874019. The device is classified under product code JWX. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAPHSLIDE?

STAPHSLIDE is a medical device that received FDA 510(k) clearance on 1987-10-28. The listed applicant is Ncs Diagnostics, Inc.. The 510(k) number is K874019.

When did STAPHSLIDE receive FDA 510(k) clearance?

STAPHSLIDE received FDA 510(k) clearance on 1987-10-28, under 510(k) number K874019.

Who is the listed applicant for STAPHSLIDE?

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 STAPHSLIDE?

The FDA product code for STAPHSLIDE is JWX.

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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.

K943498KULTSURE STARSWAB (M210), MODIFICATIONK943499KULTSURE STARSWAB(M240), MODIFICATIONK882811STREPSLIDEK881209ASO SLIDE TESTK871404KULTSUREK870231KULTSURE

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Related Devices (Code: JWX)

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.

K090964BINAXNOX STAPHYLOCOCCUS AUREUS TESTBinax, Inc.K972030STAPHYTECT PLUS/DRYSPOT STAPHYTECT PLUSOxoid , Ltd.K964315REMEL STAPH LATEX KITRemel, L.P.K945538STAPHAUREX PLUS(TM)Murex Diagnostics LimitdK926173STAPH-A-LEX(TM) SYSTEMTrinity Laboratories, Inc.K923212SLIDEX STAPH-KITBiomerieux Vitek, Inc.

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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