PERITONEAL INTRODUCER & SHEATH— 510(k) K771529
Substantially EquivalentCordis Corp.
FDA 510(k) clearance K771529 for PERITONEAL INTRODUCER & SHEATH, Substantially Equivalent on 1977-08-16. Applicant: Cordis Corp.. Device class: 1.
Clearance details
- Applicant
- Cordis Corp.
- Product code
- Code GYK
- Device class
- Class 1
- Regulation
- 21 CFR 882.4545
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.