# Primrose Medical, Inc.

- Location (FDA's records): Woburn, MA
- FDA decisions: 14 (1984–1989): 14 510(k) clearances
- Product codes: KNQ (2), KNT (1), FPA (1), BZW (1), FFP (1), FMK (1), FGE (1), GES (1), EZN (1), KZD (1), BZT (1), ODD (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
- K884715: Achelasia Balloon Dialator (Sep 29, 1989)
- K884713: Colonic Balloon Dialators (Sep 29, 1989)
- K884714: Biliary Dialator (Sep 29, 1989)
- K884711: Urethral and Ureteral Balloon Dilatators (Sep 29, 1989)
- K884709: Endoscopes & Access.(Sclerotherapy/Transbronchial) (Sep 8, 1989)
- K884712: Esophageal and Pyloric Balloon Dialators (Sep 8, 1989)
- K883420: Lancet, Blood (Aug 26, 1988)
- K881976: Catheter, Intravascular (Aug 4, 1988)

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