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FDA 510(k)

E-COLI-CHEK TUBE

K-Number: K844276 · 1984-12-13

ApplicantE-Y Laboratories, Inc.
Decision Date1984-12-13
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

E-COLI-CHEK TUBE 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 1984-12-13 under 510(k) number K844276. 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 E-COLI-CHEK TUBE?

E-COLI-CHEK TUBE is a medical device that received FDA 510(k) clearance on 1984-12-13. The listed applicant is E-Y Laboratories, Inc.. The 510(k) number is K844276.

When did E-COLI-CHEK TUBE receive FDA 510(k) clearance?

E-COLI-CHEK TUBE received FDA 510(k) clearance on 1984-12-13, under 510(k) number K844276.

Who is the listed applicant for E-COLI-CHEK TUBE?

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 E-COLI-CHEK TUBE?

The FDA product code for E-COLI-CHEK TUBE is JTO.

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 TUBESK934129STREP-A-CHEK

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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