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FDA 510(k)

CATHRA GRAM POSITIVE SCREEN

K-Number: K874606 · 1988-05-06

ApplicantMct Medical, Inc.
Decision Date1988-05-06
Product CodeLQL
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CATHRA GRAM POSITIVE SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is Mct Medical, Inc.. It received FDA 510(k) clearance on 1988-05-06 under 510(k) number K874606. The device is classified under product code LQL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHRA GRAM POSITIVE SCREEN?

CATHRA GRAM POSITIVE SCREEN is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Mct Medical, Inc.. The 510(k) number is K874606.

When did CATHRA GRAM POSITIVE SCREEN receive FDA 510(k) clearance?

CATHRA GRAM POSITIVE SCREEN received FDA 510(k) clearance on 1988-05-06, under 510(k) number K874606.

Who is the listed applicant for CATHRA GRAM POSITIVE SCREEN?

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

What is the FDA product code for CATHRA GRAM POSITIVE SCREEN?

The FDA product code for CATHRA GRAM POSITIVE SCREEN is LQL.

Related Clinical Trials

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 Mct Medical, 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.

K880504MCT MEDICAL BROWNE UROSCAN URODYNAMICK861958REPLIANALYZER

Related Devices (Code: LQL)

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.

K972576GRAM POSITIVE AUTOIDENTIFICATION PLATES, SENSITITRE AP90Accumed Intl., Inc.K961968BBLCRYSTAL GRAM-POSITIVE ID SYSTEMBd Becton Dickinson Vacutainer Systems PreanalyticK961730RAPID GRAM-POSITIVE ID SYSTEMBecton Dickinson Microbiology SystemsK952095VITEK GRAM POSITIVE IDENTIFICATION CARD (GPI)Biomerieux Vitek, Inc.K925916VITEK RAPID CALL-GRAM POSITIVE IDENTIFICATION CARDBiomerieux Vitek, Inc.K910304RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIAVitek Systems, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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