Company ยท US
Ramco Laboratories, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1998. Name variants (Inc, Corp, punctuation) are merged.
9510(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 22, 1998 | K983107 | VFE Ramco Laboratories, Inc. | GGP |
| Oct 21, 1998 | K981208 | TFR Ramco Laboratories, Inc. | JNM |
| Nov 29, 1991 | K910481 | EPO-RIA Ramco Laboratories, Inc. | GGT |
| Sep 4, 1987 | K872941 | SPECTRO C Ramco Laboratories, Inc. | GGP |
| Mar 30, 1987 | K864701 | VWF IMMUNOBLOT Ramco Laboratories, Inc. | GGP |
| May 1, 1986 | K861159 | SPECTRO VWF Ramco Laboratories, Inc. | GGP |
| Jun 22, 1983 | K831470 | PTH MR Ramco Laboratories, Inc. | CEW |
| Dec 28, 1982 | K823016 | CANDIDA DETECTION SYSTEM Ramco Laboratories, Inc. | LHK |
| Aug 12, 1981 | K812056 | SPECTRO FEIRITIN Ramco Laboratories, Inc. | DBF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||