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FDA 510(k)

VRESELECT CULTURE MEDIUM

K-Number: K103684 · 2011-10-21

ApplicantBio-Rad
Decision Date2011-10-21
Product CodeJSO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VRESELECT CULTURE MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 2011-10-21 under 510(k) number K103684. The device is classified under product code JSO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VRESELECT CULTURE MEDIUM?

VRESELECT CULTURE MEDIUM is a medical device that received FDA 510(k) clearance on 2011-10-21. The listed applicant is Bio-Rad. The 510(k) number is K103684.

When did VRESELECT CULTURE MEDIUM receive FDA 510(k) clearance?

VRESELECT CULTURE MEDIUM received FDA 510(k) clearance on 2011-10-21, under 510(k) number K103684.

Who is the listed applicant for VRESELECT CULTURE MEDIUM?

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

What is the FDA product code for VRESELECT CULTURE MEDIUM?

The FDA product code for VRESELECT CULTURE MEDIUM is JSO.

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Other records listing Bio-Rad 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.

K171061MRSASelect IIK122187VRESELECT CULTURE MEDIUMK093678PLATELIA ASPERGILLUS EIA MODEL 62793K100589MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENSK081362PLATELIA LYME IGMK081212MRSASELECT - EXTENDED INCUBATION

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Related Devices (Code: JSO)

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.

K190553HardyCHROM CREHardy DiagnosticsK181092CHROMID CARBA agar (CARB)Biomerieux S.A.K171061MRSASelect IIBio-RadK162620Remel Spectra ESBLRemel, Inc.K160512HardyCHROM ESBLHardy DiagnosticsK162076chromID MRSAbioMerieux, 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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