# K973431: Lasette

- Pathway: 510(k) (Traditional)
- Applicant: Cell Robotics, Inc.
- Decided: Oct 28, 1997 after 48 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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) Glucolet Steel Lancet: named in the summary without a submission number
- (no number) Foother Touch Steel Lancet: named in the summary without a submission number
- (no number) Tenderlett Steel lances: named in the summary without a submission number
- (no number) Trilasc 2940: named in the summary without a submission number
- (no number) Medlite: named in the summary without a submission number
- (no number) Protégé: named in the summary without a submission number

## Indications for use
The Cell Robatics Lasette Laser Skin Perforator is intended for use by qualified healthcare professionals for collecting capillary blood samples from adult patients, for subsequent determination of blood glucose concentration and hematocrit using optically based measurement techniques.

Source page: https://510kreport.com/device/K973431
Methodology: https://510kreport.com/methodology