Product code LDW— Pathology
ATS SCHAUDINN'S FIXATIVE W/ACETIC ACID
- Classification name
- Fixative, Acid Containing
- Device class
- Class 1
- Regulation
- 21 CFR 864.4010
- Advisory panel
- Pathology
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code LDW
FDA has cleared devices under product code LDW between 1983 and 1988, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1988
- 1984
- 1983
Top applicants under product code LDW
Recent clearances under product code LDW
Data sourced from openFDA. This site is unofficial and independent of the FDA.