# Dravon Medical, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 16 (1977–1987): 16 510(k) clearances
- Product codes: KDJ (3), FJS (2), KDC (1), LDR (1), DQR (1), FJZ (1), KSR (1), HQC (1), KNR (1), HTD (1), KOC (1), FJK (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
- K873455: S3086 Arterial, S3087 Venous Neonatal Hemodialysis (Sep 14, 1987)
- K860770: AM-100 I/a Ampac (Apr 21, 1986)
- K832739: Stediflo Infusion Set (Dec 22, 1983)
- K831842: Dravon T Clamp (Sep 26, 1983)
- K812772: Peritoneal Dialysis Cycler Set (8UNIT) (Oct 19, 1981)
- K812771: Peritoneal Dialysis Drainage (Oct 19, 1981)
- K811851: S-610 Shunt Adaptor Set (Aug 31, 1981)
- K800435: Hemostatic/Tube Occluding Forceps (Mar 12, 1980)

Source page: https://510kreport.com/company/dravon-medical