# Pace Tech, Inc.

- Location (FDA's records): Clearwater, FL
- FDA decisions: 18 (1988–1996): 18 510(k) clearances
- Product codes: DQA (5), MHX (4), CCK (3), DRT (2), DXN (2), DSK (1), CBS (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
- K951226: Vitalmax 4000/Minipack 3100/3000 (Nov 21, 1996)
- K953795: Vitalmax 4100 (Jul 1, 1996)
- K944541: Handypack 911SC (Feb 22, 1995)
- K945385: Vitalmax 800 Plus/Vitalmax 810 Plus/Minipack 300 (Jan 31, 1995)
- K925701: Minipack 911-STC (Aug 11, 1994)
- K934385: Minipack 3100/3000 Modification (Aug 10, 1994)
- K933624: Vitalmax 4000 (Jul 19, 1994)
- K930559: Vitalmax 800-C (Sep 3, 1993)

Source page: https://510kreport.com/company/pace-tech