EURO-MED ENDO-CURETTE— 510(k) K882606
Substantially EquivalentBuckman Co., Inc.
FDA 510(k) clearance K882606 for EURO-MED ENDO-CURETTE, Substantially Equivalent on 1988-07-25. Applicant: Buckman Co., Inc.. Device class: 2.
Clearance details
- Applicant
- Buckman Co., Inc.
- Product code
- Code PCF
- Device class
- Class 2
- Regulation
- 21 CFR 884.1050
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Martinez, CA, US
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