# Clinical Data, Inc.

- Location (FDA's records): Boston, MA
- FDA decisions: 37 (1982–2007): 37 510(k) clearances
- Names in FDA's records: Clinical Data, Inc. (36); Clinical Data (1)
- Product codes: KNK (3), DRX (3), JIY (2), CDT (2), CIG (2), CIS (1), KLS (1), JGJ (1), LBS (1), CKA (1), DSF (1), CIX (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Genzyme Corp.: 1 (https://510kreport.com/company/genzyme)

## Recent decisions
- K071706: Envoy 500 HDL; Cholesterol Reagent Kit (Model# 55301), Calibrator Kit (Model# 55118) (Dec 20, 2007)
- K052591: Nanopia Wide Range C-Reactive Protein (CRP) Reagent Kit (Feb 9, 2006)
- K033983: Vitalab Iron Reagent (May 21, 2004)
- K040631: Vitalab Direct Bilirubin Reagent (Mar 18, 2004)
- K040534: Vitalab Amylase Reagent (Mar 11, 2004)
- K034000: Vitalab Triglycerides Reagent and Vitalab Calibrator (Mar 10, 2004)
- K040467: Vitalab Uric Acid Reagent (Mar 8, 2004)
- K040508: Vitalab Magnesium Reagent (Mar 8, 2004)

Source page: https://510kreport.com/company/clinical-data