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FDA 510(k)

TRANSPORT CULTURE MEDIUM DEVICE

K-Number: K120846 · 2012-06-08

Decision Date2012-06-08
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRANSPORT CULTURE MEDIUM DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Medical Products, LLC. It received FDA 510(k) clearance on 2012-06-08 under 510(k) number K120846. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSPORT CULTURE MEDIUM DEVICE?

TRANSPORT CULTURE MEDIUM DEVICE is a medical device that received FDA 510(k) clearance on 2012-06-08. The listed applicant is Puritan Medical Products, LLC. The 510(k) number is K120846.

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

TRANSPORT CULTURE MEDIUM DEVICE received FDA 510(k) clearance on 2012-06-08, under 510(k) number K120846.

Who is the listed applicant for TRANSPORT CULTURE MEDIUM DEVICE?

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

What is the FDA product code for TRANSPORT CULTURE MEDIUM DEVICE?

The FDA product code for TRANSPORT CULTURE MEDIUM DEVICE is LIO.

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.

Other records listing Puritan Medical Products, LLC 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.

Related Devices (Code: LIO)

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.

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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