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FDA 510(k)

RUBELISA TEST KIT

K-Number: K792133 · 1980-01-11

ApplicantMicrobiological Assoc.
Decision Date1980-01-11
Product CodeGOK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

RUBELISA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Microbiological Assoc.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792133. The device is classified under product code GOK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUBELISA TEST KIT?

RUBELISA TEST KIT is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Microbiological Assoc.. The 510(k) number is K792133.

When did RUBELISA TEST KIT receive FDA 510(k) clearance?

RUBELISA TEST KIT received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792133.

Who is the listed applicant for RUBELISA TEST KIT?

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

What is the FDA product code for RUBELISA TEST KIT?

The FDA product code for RUBELISA TEST KIT is GOK.

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Other records listing Microbiological Assoc. 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.

K791397HERPES EIA TEST KITK781549TOXELISA TEST KITK780996RUBELISA TEST KITK781392CYTOMEGILISH TEST KITK781143IMMUNOFLUORESCENCE TEST KITK770764TISSUE CULTURE MEDIA W/HEPES BUFFER

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Related Devices (Code: GOK)

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.

K832228RUBASCAN LATEX CARD TESTBd Becton Dickinson Vacutainer Systems PreanalyticK810835RUBAZYME - MAbbott LaboratoriesK792635ANTIBODY TO RUBELLA VIRUSElectro-Nucleonics Laboratories, Inc.K790122RUBANONOrganon, Inc.K781638RUBINDEX*DIRECT SYSTEMOrtho Diagnostics, Inc.K781392CYTOMEGILISH TEST KITMicrobiological Assoc.

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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