# K983623: Modulap

- Pathway: 510(k) (Traditional)
- Applicant: Atc Technologies, Inc.
- Decided: Dec 18, 1998 after 64 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Nezhat-Dorsey Reusable Electrosurgical Attachments: named in the summary without a submission number
- (no number) Nezhat-Dorsey Reusable Electrosurgical Unipolar Inserts: named in the summary without a submission number

## Most influential descendants
- K132300: Epix Electrosurgical Probe Spatula Tip, Epix Electrosurgical Probe L-Hook Tip, Epix Electrosurgical Probe J-Hook Tip, RE (2014), 1 descendant of its own
- K171684: Epix Electrosurgical Probe with Smoke Evacuation (2017), 0 descendants of its own

## Indications for use
The Candidate Devices are indicated for use in patients eligible for monopolar electrosurgical treatment via general laparoscopic surgical procedures.

Source page: https://510kreport.com/device/K983623
Methodology: https://510kreport.com/methodology