WALLACH LEEP PROCEDURE KIT — Wallach Surgical Devices, Inc. (510(k) K935634)
WALLACH LEEP PROCEDURE KIT — Wallach Surgical Devices, Inc. (510(k) K935634) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: WALLACH LEEP PROCEDURE KIT; Applicant: Wallach Surgical Devices, Inc.; Clearance track: 510(k).
| Device name | WALLACH LEEP PROCEDURE KIT |
|---|---|
| Applicant | Wallach Surgical Devices, Inc. |
| Clearance track | 510(k) |
| Submission number | K935634 |
| Decision | Substantially Equivalent |
| Decision date | 1994-07-20 |
| Date received | 1993-11-23 |
| Product code | HGI |
| Device class | 2 |
| Medical specialty | Obstetrics/Gynecology |
| Applicant location | CT, US |
| Source | openFDA device |
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