AUTO SUTURE CHEMOSITE TUNNELER— 510(k) K961856
Substantially EquivalentUnited States Surgical, A Division of Tyco Healthc
FDA 510(k) clearance K961856 for AUTO SUTURE CHEMOSITE TUNNELER, Substantially Equivalent on 1996-07-18. 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 LJS
- Device class
- Class 2
- Regulation
- 21 CFR 880.5970
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Norwalk, CT, US
Recent devices under product code LJS
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- K252792 — PM2 System with ECGuide Connector
- K243458 — HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301) +5 more
- K251212 — Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)
More clearances from United States Surgical, A Division of Tyco Healthc
view allAdverse events under product code LJS
product code LJS- Death
- 31
- Injury
- 2,791
- Malfunction
- 18,374
- Other
- 5
- Total
- 21,201
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.