Product code LQS— Unknown
MENTOR ALLOPLASTIC SPERMATOCELE
- Classification name
- Spermatocele, Alloplastic
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code LQS
FDA has cleared device under product code LQS, all in 1986, filed by 1 applicant company. No FDA device recalls reference this product code.
Top applicants under product code LQS
Recent clearances under product code LQS
Data sourced from openFDA. This site is unofficial and independent of the FDA.