# K992714: Micrograsp Monopolar Coagulator, Model Nos 90001-90010

- Pathway: 510(k) (Traditional)
- Applicant: Hysterx, Inc.
- Decided: Oct 5, 1999 after 54 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K922802 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922802: Microsurge Front-End Grasping Devices, Microsurge, Inc. (1993) Summary page 1.

## Indications for use
The MicroGRASP Monopolar Coagulator is indicated for use in the grasping and coagulation of soft tissue and blood vessels up to 3 mm during open and guidance-assisted surgical procedures.

Source page: https://510kreport.com/device/K992714
Methodology: https://510kreport.com/methodology