Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH)

FDA 510(k) K190485 · Kawasumi Laboratories, Inc.

Substantially Equivalent

510(k) numberK190485

Submission

Device name
Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH)
Applicant
Kawasumi Laboratories, Inc.
Tokyo, JP
Received
February 27, 2019
Decision date
July 8, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1675
Specialty
Clinical Chemistry

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Questions and answers

When was Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) cleared by the FDA?

Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) (K190485) received a 510(k) decision of Substantially Equivalent on July 8, 2019, 131 days after the submission was received.

What is the product code of K190485?

The FDA product code is JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection, a Class II (moderate risk) device regulated under 21 CFR 862.1675.