# Intercare Diagnostics, Inc.

- Location (FDA's records): Baltimore, MD
- FDA decisions: 5 (1986–1994): 5 510(k) clearances
- Product codes: LSQ (2), HCC (1), JPK (1), LJC (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K941938: The Mirage System Biofeedback Interface (Aug 5, 1994)
- K920569: Indxtm Dip-S-Tickstm (Feb 9, 1993)
- K901597: Indx Dip S Ticks (Dec 21, 1990)
- K893895: Hematology Control Mixtures for Quality Control (Jul 25, 1989)
- K862948: Chlamydia Tissue Culture Confirmation Test (Eia) (Oct 17, 1986)

Source page: https://510kreport.com/company/intercare-diagnostics
