# K013701: Endo-Glide

- Pathway: 510(k) (Traditional)
- Applicant: Sonotech, Inc.
- Decided: Feb 4, 2002 after 88 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
Longest line of descent: 1 generation back to K780386 (1978). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984562: Vivosonic, Sonotech, Inc. (1999) Summary page 1.
- K780386: K-Y Lubricating Jelly, Johnson & Johnson Professionals, Inc. (1978) Summary page 1.
- K810310: K-Y Lubricating Jelly, Johnson & Johnson Professionals, Inc. (1981) Summary page 1.
- (no number) Surgilube: named in the summary without a submission number

## Indications for use
Lubricate the insertion and passage of imaging devices and surgical instrumentation, such as endoscopes, ultrasound transducers, transesophageal echocardiography (TEE) transducers, catheters and surgical instrumentation.

Source page: https://510kreport.com/device/K013701
Methodology: https://510kreport.com/methodology