PPA/BT-RB STETHOSCOPE— 510(k) K132405
Substantially EquivalentRnk Products, Inc.
FDA 510(k) clearance K132405 for PPA/BT-RB STETHOSCOPE, Substantially Equivalent on 2013-10-11. Applicant: Rnk Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Rnk Products, Inc.
- Product code
- Code DQD
- Device class
- Class 2
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Melbourne, FL, US
Recent devices under product code DQD
view allMore clearances from Rnk Products, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.