Company ยท US
Foley & Lardner
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1998. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Apr 14, 1998 | K973613 | CH-611B AND CH-611C DIGITAL WRIST SPHYGMOMANOMETERS BLOOD PRESSURE METER Foley & Lardner | DXN |
| Nov 7, 1994 | K942311 | DYNASTY U1-33 AGM Foley & Lardner | KNN |
| Nov 7, 1994 | K942310 | DYNASTY GC 12550 (GELL/CELL) Foley & Lardner | KNN |
| Nov 7, 1994 | K942309 | DYNASTY U1-31 (GELL/CELL) Foley & Lardner | KNN |
| Nov 7, 1994 | K942308 | DYNASTY GC 12400 (GELL/CELL) Foley & Lardner | KNN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||