DYNACYT BIOPSY ASPIRATION DEVICE— 510(k) K922919
Substantially EquivalentBuckman Co., Inc.
FDA 510(k) clearance K922919 for DYNACYT BIOPSY ASPIRATION DEVICE, Substantially Equivalent on 1993-03-31. Applicant: Buckman Co., Inc..
Clearance details
- Applicant
- Buckman Co., Inc.
- Product code
- Code MJG
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.