# K881680: Ackrad H/S Procedure Tray

- Pathway: 510(k) (Traditional)
- Applicant: Ackrad Laboratories
- Decided: Jul 15, 1988 after 87 days
- Product code: HIG (Insufflator, Hysteroscopic)
- Device class: 2
- Regulation: 21 CFR 884.1700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 1 cites it directly.
0 of 9 devices 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.

## Most influential descendants
- K020954: H/S Procedure Tray (5F), H/S Procedure Tray (7F), H/S Elliptosphere Procedure Tray & Multipurpose Procedure Tray (2002), 7 descendants of its own
- K110288: Femvue Saline-Air Device (2011), 5 descendants of its own
- K241693: FemChec Controlled Saline-Air Device (FCD-250) (2024), 1 descendant of its own
- K253403: FemVue® Controlled Saline-Air Device (FSA-300) (2025), 0 descendants of its own
- K242002: FemVue MINI Saline-Air Device (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K881680
Methodology: https://510kreport.com/methodology