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FDA 510(k)

VERI-STAPH

K-Number: K830783 · 1983-04-08

ApplicantZeus Technologies
Decision Date1983-04-08
Product CodeJWX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VERI-STAPH is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Technologies. It received FDA 510(k) clearance on 1983-04-08 under 510(k) number K830783. 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 VERI-STAPH?

VERI-STAPH is a medical device that received FDA 510(k) clearance on 1983-04-08. The listed applicant is Zeus Technologies. The 510(k) number is K830783.

When did VERI-STAPH receive FDA 510(k) clearance?

VERI-STAPH received FDA 510(k) clearance on 1983-04-08, under 510(k) number K830783.

Who is the listed applicant for VERI-STAPH?

The FDA 510(k) record lists Zeus Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERI-STAPH?

The FDA product code for VERI-STAPH is JWX.

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Other records listing Zeus Technologies 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.

K840012INDIRECT FLUORESCENT ANTIBODY MYCOK831026INDIRECT FLUORESCENT ANTIBODY REAGENTSK822859DIRECT FA CONJUGATE FOR LEGIONELLA SPP

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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