Company ยท US
Lares Manufacturing Co., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1983. 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 |
|---|---|---|---|
| Nov 14, 1983 | K831351 | PERMALUX VISIBLE CURE COMPOSITE RESTOR Lares Manufacturing Co., Inc. | EBF |
| Dec 16, 1980 | K801535 | LARES HANDPIECE OIL Lares Manufacturing Co., Inc. | EFB |
| Jul 21, 1980 | K801592 | FIBER OPTIC HOSE Lares Manufacturing Co., Inc. | EAY |
| Jul 21, 1980 | K801591 | FIBER OPTIC ILLUMINATOR Lares Manufacturing Co., Inc. | EAY |
| Jul 14, 1980 | K801534 | LARES AIR PRESSURE GAUGE Lares Manufacturing Co., Inc. | EIA |
| Jan 20, 1978 | K780038 | DENTAL HANDPIECE Lares Manufacturing Co., Inc. | EFB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||