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FDA 510(k)

MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM

K-Number: K032246 · 2003-08-13

ApplicantStarplex Scientific, Inc.
Decision Date2003-08-13
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Starplex Scientific, Inc.. It received FDA 510(k) clearance on 2003-08-13 under 510(k) number K032246. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM?

MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM is a medical device that received FDA 510(k) clearance on 2003-08-13. The listed applicant is Starplex Scientific, Inc.. The 510(k) number is K032246.

When did MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM received FDA 510(k) clearance on 2003-08-13, under 510(k) number K032246.

Who is the listed applicant for MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM?

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

What is the FDA product code for MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM?

The FDA product code for MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEM is JSM.

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Other records listing Starplex Scientific, Inc. as applicant

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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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