Company ยท US
Kawasumi Laboratories America, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2010. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 21, 2010 | K102890 | K-SHIELD SMALL VEIN INFUSION / WINGED COLLECTION SET W/ ANTI NEEDLE STICK PROTECTOR (AND MULTISAMPLE LUER ADAPTER) Kawasumi Laboratories America, Inc. | FPA |
| Apr 15, 2003 | K030385 | IV ADD-ON FILTER ADMINISTRATION SET WITH AND WITHOUT Y CONNECT OR NEEDLELESS ACCESS CONNECTOR Kawasumi Laboratories America, Inc. | FPA |
| Jul 21, 2000 | K001426 | KAWASUMI LABORATORIES IV ADMINISTRATION SET WITH FILTER Kawasumi Laboratories America, Inc. | FPA |
| Jul 21, 2000 | K001424 | KAWASUMI LABORATORIES IV ADMINISTRATION SET, STANDARD Kawasumi Laboratories America, Inc. | FPA |
| Jul 21, 2000 | K001423 | KAWASUMI LABORATORIES IV ADMINISTRATION SET, PRIMARY Kawasumi Laboratories America, Inc. | FPA |
| May 19, 2000 | K001043 | KAWASUMI LABORATORY BLOOD DRAWING KIT Kawasumi Laboratories America, Inc. | KSB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||