# K973146: Mentor Super Absorbent Drape

- Pathway: 510(k) (Traditional)
- Applicant: Mentor Ophthalmics, Inc.
- Decided: Dec 4, 1997 after 104 days
- Product code: KKX (Drape, Surgical, Antimicrobial)
- Device class: 2
- Regulation: 21 CFR 878.4370
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) American Threshold Disposable OR Towel: named in the summary without a submission number
- (no number) Johnson & Johnson Sof-Wick Lap Pad: named in the summary without a submission number

## Indications for use
The Super Absorbent Drape is used to absorb fluids during surgical procedures.

Source page: https://510kreport.com/device/K973146
Methodology: https://510kreport.com/methodology