K073705

Substantially Equivalent

MODEL TW SB, SCALP VEIN SET; MODEL TW LB, STERILE HYPODERMIC NEEDLE

Applicant: Shandong Qiaopai Group Co., Ltd.
Product code: FMI
Advisory panel: General Hospital
Date received: 2007-12-31
Decision date: 2008-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zibo, CN

Adverse events under product code FMI

product code FMI

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 →

Data sourced from openFDA. This site is unofficial and independent of the FDA.