# Spencer Fillmore

- Location (FDA's records): San Francisco, CA
- FDA decisions: 3 (2013–2014): 3 510(k) clearances
- Product codes: JAQ (3)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Varian Medical Systems, Inc.: 2 (https://510kreport.com/company/varian-medical-systems)
- Mick Radio-Nuclear Instruments, Inc.: 2 (https://510kreport.com/company/mick-radio-nuclear-instruments)

## Firms that cite its devices most
- Kobold, LLC: 3 (https://510kreport.com/company/kobold)

## Its most-cited devices
- K123912: Kobold Fletcher Type Applicator Set, Kobold Henschke Type Applicator Set (2013), cited by 2
- K123941: Kobold Sure-Guide Vaginal Cylinder Set, Stump Vaginal Cylinder Set, Miami Cylinder Set (2013), cited by 1

## Recent decisions
- K130757: Kobold Secure Lock Transfer Guide Tube Set; Kobold Luer Transfer Guide Tube Set (Apr 3, 2014)
- K123912: Kobold Fletcher Type Applicator Set, Kobold Henschke Type Applicator Set (May 14, 2013)
- K123941: Kobold Sure-Guide Vaginal Cylinder Set, Stump Vaginal Cylinder Set, Miami Cylinder Set (Apr 30, 2013)

Source page: https://510kreport.com/company/spencer-fillmore