SKYLARK MODEL 1001 TENS DEVICE— 510(k) K853898
Substantially EquivalentPeleg Intl. Co.
FDA 510(k) clearance K853898 for SKYLARK MODEL 1001 TENS DEVICE, Substantially Equivalent on 1986-06-18. Applicant: Peleg Intl. Co..
Clearance details
- Applicant
- Peleg Intl. Co.
- Product code
- Code GZJ
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Canada, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.