# K951123: Cavicide Surface Disinfectant/Decontaminant Cleaner

- Pathway: 510(k) (Traditional)
- Applicant: Micro-Aseptic Products, Inc.
- Decided: Apr 25, 1995 after 60 days
- Product code: LRJ (Disinfectant, Medical Devices)
- Device class: 1
- Regulation: 21 CFR 880.6890
- 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
- Feb 6, 2012 · Class II · Z-2267-2012: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance because the affected lot of product containing this fragance has caused an increase in reported health reactions in some ind

Source page: https://510kreport.com/device/K951123
Methodology: https://510kreport.com/methodology