MULTI-SAMPLE LUER ADAPTER FOR BLOOD SAMPLE COLLECTION— 510(k) K935506

Clearance details

Applicant

Kawasumi Laboratories Co., Ltd.

Product code

Code FMI

Device class

Class 2

Regulation

21 CFR 880.5570

Advisory panel

General Hospital

Date received

1993-11-16

Decision date

1994-02-03

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Tokyo, JP

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• K935514 — VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER1994-02-10
• K935505 — WINGED COLLECTION SET W/MULTI-SAMPLE LUER ADAPTER1994-02-03

Death

28

Injury

1,517

Malfunction

23,981

Other

18

Total

25,544

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →