Company ยท US
Greer Laboratories, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2000. Name variants (Inc, Corp, punctuation) are merged.
2510(k) clearances (0 in 12 months)
3recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 30, 2022 | Greer Laboratories, Inc. GREER DIA - KIT ANTIGEN M. FAENI, 2.0mL 20 MG/ML, Analyte Specific Reagent, Item: K62, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies. Terminated |
DGW | None listed |
| Nov 30, 2022 | Greer Laboratories, Inc. GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies. Terminated |
DGW | None listed |
| Mar 1, 2005 | Greer Laboratories Inc Sterile Empty Vials for Allergenic Extracts, 100ml size Terminated |
JKA | None listed |