THE KLINE APPLICATOR— 510(k) K823517
Substantially EquivalentKline Technologies, Ltd.
FDA 510(k) clearance K823517 for THE KLINE APPLICATOR, Substantially Equivalent on 1983-01-18. Applicant: Kline Technologies, Ltd.. Device class: 1.
Clearance details
- Applicant
- Kline Technologies, Ltd.
- Product code
- Code HGD
- Device class
- Class 1
- Regulation
- 21 CFR 884.4520
- Advisory panel
- Obstetrics/Gynecology
- 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.