ANCHOR BRAND SURGICAL NEEDLES— 510(k) K831648
Substantially EquivalentAnchor Products Co.
FDA 510(k) clearance K831648 for ANCHOR BRAND SURGICAL NEEDLES, Substantially Equivalent on 1983-08-16. Applicant: Anchor Products Co..
Clearance details
- Applicant
- Anchor Products Co.
- Product code
- Code GAB
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.