# K030838: Wartner Pro

- Pathway: 510(k) (Traditional)
- Applicant: Wartner Medical Products
- Decided: Jun 27, 2003 after 102 days
- Product code: GEH (Unit, Cryosurgical, Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4350
- 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) Wartner Wart Removal System for OTC use: named in the summary without a submission number
- (no number) Histofreezer Portable Cryosurgical Unit: named in the summary without a submission number
- (no number) Tinamed Plantar Patch: named in the summary without a submission number
- (no number) Tinamed Wart Remover indicated for common warts and plantar warts: named in the summary without a submission number
- (no number) Maximum Strength Wart-Off: named in the summary without a submission number
- (no number) DuoFilm Salicylic Acid Wart Remover indicated for common warts and plantar warts: named in the summary without a submission number
- (no number) Clear Away System Plantar Wart Remover for Feet: named in the summary without a submission number

## Indications for use
WARTNER PRO® is intended for the treatment of common warts and plantar warts.

Source page: https://510kreport.com/device/K030838
Methodology: https://510kreport.com/methodology