# Advanced Sterilization Products (Asp)

- Location (FDA's records): Irvin, CA
- FDA decisions: 5 (2016–2020): 5 510(k) clearances
- Product codes: FRC (3), FEB (2)
- 510(k) review time since 2016: median 166 days, against 130 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 9 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Advanced Sterilization Products: 2 (https://510kreport.com/company/advanced-sterilization-products)
- 3M Company: 2 (https://510kreport.com/company/3m)
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)
- Albert Browne, Ltd.: 1 (https://510kreport.com/company/albert-browne)
- STERIS Corporation: 1 (https://510kreport.com/company/steris)

## Firms that cite its devices most
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- Advanced Sterilization Products: 1 (https://510kreport.com/company/advanced-sterilization-products)

## Its most-cited devices
- K170039: STERRAD VELOCITY Biological Indictator and Reader (2017), cited by 1
- K182404: STERRAD VELOCITY Biological Indicator (2018), cited by 1
- K192025: STERRAD VELOCITY Biological Indicator/Process Challenge Device and Reader (2020), cited by 1
- K152189: Evotech Ecr (2016), cited by 1

## Recent decisions
- K192025: STERRAD VELOCITY Biological Indicator/Process Challenge Device and Reader (Jan 23, 2020)
- K181472: AEROFLEX (TM) Automatic Endoscope Reprocessor with AUTOSURE (TM) MRC Monitor (Apr 23, 2019)
- K182404: STERRAD VELOCITY Biological Indicator (Dec 27, 2018)
- K170039: STERRAD VELOCITY Biological Indictator and Reader (Jun 20, 2017)
- K152189: Evotech Ecr (Jul 20, 2016)

Source page: https://510kreport.com/company/advanced-sterilization-products-asp