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FDA 510(k)

STREP-A-CHEK

K-Number: K934129 · 1994-08-26

ApplicantE-Y Laboratories, Inc.
Decision Date1994-08-26
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

STREP-A-CHEK is the device name listed in this FDA 510(k) record. The listed applicant is E-Y Laboratories, Inc.. It received FDA 510(k) clearance on 1994-08-26 under 510(k) number K934129. 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 STREP-A-CHEK?

STREP-A-CHEK is a medical device that received FDA 510(k) clearance on 1994-08-26. The listed applicant is E-Y Laboratories, Inc.. The 510(k) number is K934129.

When did STREP-A-CHEK receive FDA 510(k) clearance?

STREP-A-CHEK received FDA 510(k) clearance on 1994-08-26, under 510(k) number K934129.

Who is the listed applicant for STREP-A-CHEK?

The FDA 510(k) record lists E-Y Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STREP-A-CHEK?

The FDA product code for STREP-A-CHEK is JTO.

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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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Other records listing E-Y Laboratories, 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.

K934130SWABZYME OXIDASEK940162GONOCHEK II REAGENT TUBESK940161B-LACTAMASE REAGENT TUBESK934125GONOCHEK-II, MODIFICATIONK940124EY-20 REAGENT TUBESK940020STREP-A-CHEK(TM) REAGENT STRIPS

View all 13 devices →

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.

K050352IN-VITRO DIAGNOSTIC VAGINITIS TEST KITAmeritek Research, LLCK970832PYR SWABRemel, Inc.K970834GRAM SWABRemel, Inc.K970833INDOLE SWABRemel, Inc.K970009LYFO(TM) DIFFERENTIAL DISK-BACITRACINMicrobiologics, Inc.K962966IDS RAPID CB PLUS SYSTEMInnovative Diagnostic Systems, 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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