Allison Medical, Inc.
Allison Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1999, with 2 FDA device recalls on record.
Top product codes for Allison Medical, Inc.
FDA recalls by Allison Medical, Inc.
- Z-0478-2023 — CarePoint 60 mL Syringe Without Needle, REF: 04-7560
- Z-0266-2023 — InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Allison Medical, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.