MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE— 510(k) K860102
Substantially EquivalentEndotherapeutics
FDA 510(k) clearance K860102 for MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE, Substantially Equivalent on 1986-02-12. Applicant: Endotherapeutics.
Clearance details
- Applicant
- Endotherapeutics
- Product code
- Code FHP
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redwood City, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.