← Product Code [GEH](/submissions/SU/subpart-e%E2%80%94surgical-devices/GEH) · K960387

# UROSPROBE SYSTEM, MODEL 1000 (K960387)

_Uros Corp. · GEH · Apr 1, 1996 · General, Plastic Surgery · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GEH/K960387

## Device Facts

- **Applicant:** Uros Corp.
- **Product Code:** [GEH](/submissions/SU/subpart-e%E2%80%94surgical-devices/GEH.md)
- **Decision Date:** Apr 1, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 878.4350
- **Device Class:** Class 2
- **Review Panel:** General, Plastic Surgery

## Regulatory Identification

(1) Cryosurgical unit with a liquid nitrogen cooled cryoprobe and accessories. A cryosurgical unit with a liquid nitrogen cooled cryoprobe and accessories is a device intended to destroy tissue during surgical procedures by applying extreme cold. (2) Cryosurgical unit with a nitrous oxide cooled cryoprobe and accessories. A cryosurgical unit with a nitrous oxide cooled cryoprobe and accessories is a device intended to destroy tissue during surgical procedures, including urological applications, by applying extreme cold. (3) Cryosurgical unit with a carbon dioxide cooled cryoprobe or a carbon dioxide dry ice applicator and accessories. A cryosurgical unit with a carbon dioxide cooled cryoprobe or a carbon dioxide dry ice applicator and accessories is a device intended to destroy tissue during surgical procedures by applying extreme cold. The device is intended to treat disease conditions such as tumors, skin cancers, acne scars, or hemangiomas (benign tumors consisting of newly formed blood vessels) and various benign or malignant gynecological conditions affecting vulvar, vaginal, or cervical tissue. The device is not intended for urological applications.

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**Source:** [https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GEH/K960387](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/GEH/K960387)

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