Home › Device types › LDM
Instrumentation, High Pressure Liquid Chromatography
FDA product code LDM · Class 1 · Clinical Chemistry
22
Registered devices
7
Adverse events
1
Recalls
19
510(k) clearances
Devices with this code
D-10 — BIO-RAD LABORATORIES, INC.D-100 — BIO-RAD LABORATORIES, INC.Acquity — WATERS TECHNOLOGIES CORPORATIONHemoglobin Variants System — BIO-RAD LABORATORIES, INC.D-10 — BIO-RAD LABORATORIES, INC.Acquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIOND-10 — BIO-RAD LABORATORIES, INC.VARIANT II — BIO-RAD LABORATORIES, INC.Acquity — WATERS TECHNOLOGIES CORPORATIONVARIANT II TURBO — BIO-RAD LABORATORIES, INC.Acquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONHemoglobin Variants System — BIO-RAD LABORATORIES, INC.Acquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATIONAcquity — WATERS TECHNOLOGIES CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-11-17 | Abbott Health Products, Inc. | Drug product cross reacts with the Tricyclic Antidepressants (TCA) assay. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
