# K020824: Speedband Superview Super 7, Injection Speedband Superview Super 7, Models 4205 and 4238

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corp
- Decided: Apr 12, 2002 after 29 days
- Product code: FHN (Ligator, Hemorrhoidal)
- Device class: 2
- Regulation: 21 CFR 876.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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) Modified Injection Speedband™ Superview: named in the summary without a submission number
- (no number) Modified Speedband™ Superview: named in the summary without a submission number

## Most influential descendants
- K101428: Otsc (Over-the Scope-Clip) System Set (2010), 6 descendants of its own
- K120814: Padlock Clip-12 (2012), 2 descendants of its own
- K241858: BARS Set (100.60) (2024), 1 descendant of its own
- K180689: Padlock Clip defect closure device; Padlock Clip Pro-Select defect closure device (2018), 1 descendant of its own
- K251562: OTSCneo System Set (100.03n-14n, 100.27n-31n) (2025), 0 descendants of its own

## Indications for use
The Speedband™ Superview Super7 is indicated for use in endoscopic ligation of esophageal varices and anorectal hemorrhoids. The Injection Speedband™ Superview Super7 is indicated for use in endoscopic treatment of esophageal varices utilizing combination ligation/injection therapy. The Injection Speedband™ Superview Super7 is also indicated for band ligation treatment of anorectal hemorrhoids.

Source page: https://510kreport.com/device/K020824
Methodology: https://510kreport.com/methodology