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FDA 510(k)

TRANSPORTER VIRAL TRANSPORT MEDIUM

K-Number: K840744 · 1984-06-07

ApplicantBartels Immunodiagnostic Supplies, Inc.
Decision Date1984-06-07
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TRANSPORTER VIRAL TRANSPORT MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Bartels Immunodiagnostic Supplies, Inc.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K840744. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSPORTER VIRAL TRANSPORT MEDIUM?

TRANSPORTER VIRAL TRANSPORT MEDIUM is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Bartels Immunodiagnostic Supplies, Inc.. The 510(k) number is K840744.

When did TRANSPORTER VIRAL TRANSPORT MEDIUM receive FDA 510(k) clearance?

TRANSPORTER VIRAL TRANSPORT MEDIUM received FDA 510(k) clearance on 1984-06-07, under 510(k) number K840744.

Who is the listed applicant for TRANSPORTER VIRAL TRANSPORT MEDIUM?

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

What is the FDA product code for TRANSPORTER VIRAL TRANSPORT MEDIUM?

The FDA product code for TRANSPORTER VIRAL TRANSPORT MEDIUM is KIT.

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Other records listing Bartels Immunodiagnostic Supplies, 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.

K864776A549 (HUMAN LUNG CARCINOMA) CULTURE CELLSK861172ROTAVIRUS LATEX AGGLUTINATION ASSAYK860279CYTOMEGALOVIRUS DIRECT FLUORESCENT ANTIBODY KITK855034AMERICAN HISTO-ID SYS PRIMARY KIT PSA PROSTATE ANTK842830IMMUNOPER-OXIDASE TEST KIT FOR DETECT OFK852185RESPIRATORY SYNCYTIAL VIRUS DIRECT FLUORESCENT ANT

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Related Devices (Code: KIT)

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.

K892938AMNIO-GROW TMInovar Biologicals, Inc.K890700MELANOCYTE GROWTH MEDIUM (MGM)Clonetics Corp.K890701ENDOTHELIAL GROWTH MEDIUM (EGM)Clonetics Corp.K890482ABC, ABC-1X, ABC(TM)Cell Ent., Inc.K884654ALPHACALF SERUMHyclone Laboratories, Inc.K884572RPMI-1640 HYBRI-MAX, PROD. NO. R5382Sigma Chemical Co.

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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