MODIFIED VERSAPORT— 510(k) K954108
Substantially EquivalentUnited States Surgical, A Division of Tyco Healthc
FDA 510(k) clearance K954108 for MODIFIED VERSAPORT, Substantially Equivalent on 1995-10-17. Applicant: United States Surgical, A Division of Tyco Healthc. Device class: 2.
Clearance details
- Applicant
- United States Surgical, A Division of Tyco Healthc
- Product code
- Code GCJ
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norwalk, CT, US
Recent devices under product code GCJ
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- K261139 — VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)
- K253541 — EZ-Close (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)
- K261614 — LED LCD Monitor (OEV-271H)
- K261249 — Universal Seal (5-12 mm)
More clearances from United States Surgical, A Division of Tyco Healthc
view allAdverse events under product code GCJ
product code GCJ- Death
- 39
- Injury
- 1,638
- Malfunction
- 28,216
- Other
- 11
- Total
- 29,904
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.