# The Timeter Group

- Location (FDA's records): Lancaster, PA
- FDA decisions: 4 (1985–1987): 4 510(k) clearances
- Product codes: CAN (1), KFZ (1), FLN (1), CAX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Alexander Mfg. Co.: 1 (https://510kreport.com/company/alexander-mfg)

## Its most-cited devices
- K844556: KHM 2000 Drip Watcher (1985), cited by 1

## Recent decisions
- K871452: Classic (TM) 200 Oxygen Flowmeter (Jun 22, 1987)
- K862171: MP-500 Electronic Nebulizer (Jul 14, 1986)
- K852374: Oxygen Regulators #50 PRT & BGT (BGT15,BGT18 (Jul 12, 1985)
- K844556: KHM 2000 Drip Watcher (Jan 14, 1985)

Source page: https://510kreport.com/company/timeter-group