# Life Design Systems, Inc.

- Location (FDA's records): Milwaukee, WI
- FDA decisions: 29 (1982–1992): 29 510(k) clearances
- Product codes: BTM (7), BYE (3), CAI (3), BSJ (3), BZO (2), CAH (2), BTC (1), BZE (1), CBP (1), DRX (1), BYD (1), DQA (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K913714: Modification Manual Pulmon Resuscitor/Pulmanex (TM) (Dec 1, 1992)
- K885313: Humidi-Flex TM (Oct 11, 1989)
- K893030: Child Size - Filter Flex (TM) (Sep 18, 1989)
- K892862: Flex-Cup Percussor (May 25, 1989)
- K892221: Pulmonary Resuscitator, Modification (May 18, 1989)
- K890011: Oxygen Connector and Oxygen Delivery Tubing (Mar 20, 1989)
- K890108: Modified Cushion-Flex (TM) (Jan 24, 1989)
- K884387: Cushion Flex (TM) (Nov 17, 1988)

Source page: https://510kreport.com/company/life-design-systems