PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCAR— 510(k) K971334
Substantially EquivalentPilling Weck Group
FDA 510(k) clearance K971334 for PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCAR, Substantially Equivalent on 1997-06-11. Applicant: Pilling Weck Group. Device class: 2.
Clearance details
- Applicant
- Pilling Weck Group
- 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
- Jeffrey, NH, US
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More clearances from Pilling Weck Group
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.