PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE) — Surgicot, Inc. (510(k) K962605)
PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE) — Surgicot, Inc. (510(k) K962605) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE); Applicant: Surgicot, Inc.; Clearance track: 510(k).
| Device name | PRO-GUARD DOUBLE-DUTY STERILIZATION WRAP (SINGLE USE) |
|---|---|
| Applicant | Surgicot, Inc. |
| Clearance track | 510(k) |
| Submission number | K962605 |
| Decision | Substantially Equivalent |
| Decision date | 1997-03-11 |
| Date received | 1996-07-02 |
| Product code | FRG |
| Device class | 2 |
| Medical specialty | General Hospital |
| Applicant location | NC, US |
| Source | openFDA device |
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