Company ยท US
Sakura Finetek U.S.A., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1989. Name variants (Inc, Corp, punctuation) are merged.
4510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 7, 1989 | K893811 | SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM Sakura Finetek U.S.A., Inc. | JQW |
| Jul 28, 1988 | K882881 | SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER Sakura Finetek U.S.A., Inc. | KES |
| Jul 1, 1988 | K881165 | SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSOR Sakura Finetek U.S.A., Inc. | IEO |
| Jan 5, 1988 | K874897 | SAKURA DRS-60 AUTOMATIC SLIDE STAINER Sakura Finetek U.S.A., Inc. | KPA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 10, 2014 | Sakura Finetek USA Inc Tissue-Tek PARAFORM PROC/EMB/MEDIUM, FORMULA 3 - 8x1Kg.
for diagnostic chemistry use.
Sakura Finetek USA, Inc. Terminated |
KEO | None listed |