FDA 510(k)

VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER

K-Number: K935514 · 1994-02-10

ApplicantKawasumi Laboratories Co., Ltd.

Decision Date1994-02-10

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Kawasumi Laboratories Co., Ltd.. It received FDA 510(k) clearance on 1994-02-10 under 510(k) number K935514. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER?

VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER is a medical device that received FDA 510(k) clearance on 1994-02-10. The listed applicant is Kawasumi Laboratories Co., Ltd.. The 510(k) number is K935514.

When did VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER receive FDA 510(k) clearance?

VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER received FDA 510(k) clearance on 1994-02-10, under 510(k) number K935514.

Who is the listed applicant for VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER?

The FDA 510(k) record lists Kawasumi Laboratories Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER?

The FDA product code for VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER is FMI.

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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.