# K854631: Assert EO Biological Test Pack

- Pathway: 510(k) (Traditional)
- Applicant: Surgicot, Inc.
- Decided: May 27, 1986 after 190 days
- Product code: FRC (Indicator, Biological Sterilization Process)
- Device class: 2
- Regulation: 21 CFR 880.2800
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Sep 10, 2013 · Class II · Z-0605-2014: STERIS has identified that the population of the G. stearothermophilus spores that monitor STEAM sterilization cycles does not meet specifications for Lot # 131004 of the Verify Dual Species Self-Cont

Source page: https://510kreport.com/device/K854631
Methodology: https://510kreport.com/methodology
