ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE— 510(k) K874585
Substantially EquivalentAngiomed U.S., Inc.
FDA 510(k) clearance K874585 for ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE, Substantially Equivalent on 1987-12-02. Applicant: Angiomed U.S., Inc..
Clearance details
- Applicant
- Angiomed U.S., Inc.
- Product code
- Code DWO
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Anaheim, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.