510(k) K821540
K821540 is an FDA 510(k) premarket notification submitted by Volu Sol Medical Industries for the device "HEMATOXYLIN II". The FDA issued a decision of Substantially Equivalent on June 10, 1982. The device falls under product code HYJ (Hematoxylin), a Class I device regulated under 21 CFR 864.1850. Volu Sol Medical Industries has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 10, 1982
- Date Received
- May 24, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Hematoxylin
- Device Class
- Class I
- Regulation Number
- 864.1850
- Review Panel
- PA
- Submission Type