Greer Laboratories, Inc.
Greer Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2000, with 2 FDA device recalls on record.
Top product codes for Greer Laboratories, Inc.
FDA recalls by Greer Laboratories, Inc.
- Z-0347-2023 — 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.
- Z-0348-2023 — 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.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Greer Laboratories, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.