# Medi-Tech, Inc.

- Location (FDA's records): Watertown, MA
- FDA decisions: 36 (1978–1996): 36 510(k) clearances
- Product codes: KNT (3), DTK (3), DIF (3), DQY (2), DQO (2), DQX (2), LIT (2), KNS (1), KOD (1), KMF (1), GBA (1), KOE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 8 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Sunwei Tech Co., Ltd.: 1 (https://510kreport.com/company/sunwei-tech)
- Therox, Inc.: 1 (https://510kreport.com/company/therox)
- Flowmedica, Inc.: 1 (https://510kreport.com/company/flowmedica)
- Boston Scientific, Target: 1 (https://510kreport.com/company/boston-scientific-target)

## Its most-cited devices
- K883880: Katzen Thrombolysis Guidewire (1989), cited by 2
- K781772: Catheter, Transluminal Balloon (1979), cited by 1
- K874096: Titanium Greenfield Vena Cava Filter Carrier (1988), cited by 1

## Recent decisions
- K954457: Medi-Tech Eddy Intravascular Infusion Catheter (May 15, 1996)
- K952345: Medi-Tech Platform Guide Catheter (Aug 17, 1995)
- K952056: Immunoassay Drugs of Abuse Controls (Jun 1, 1995)
- K945289: Doa - Immunoassay Cut-Off Calibrator (Dec 13, 1994)
- K942551: Therapeutic Drug Monitoring Control, Assayed (Oct 6, 1994)
- K943290: Bilirubin Plus/Pediatric Controls (Sep 14, 1994)
- K922990: Hemodialysis Bath (Sep 12, 1994)
- K942552: Therapeutic Drug Monitoring Control, Unassayed (Sep 9, 1994)

Source page: https://510kreport.com/company/medi-tech