510(k) K842730
K842730 is an FDA 510(k) premarket notification submitted by E K Ind., Inc. for the device "GENTIAN VIOLET". The FDA issued a decision of Substantially Equivalent on Aug 3, 1984. The device falls under product code ICF (Crystal Violet For Histology), a Class I device regulated under 21 CFR 864.1850. E K Ind., Inc. has 49 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 3, 1984
- Date Received
- Jul 13, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Crystal Violet For Histology
- Device Class
- Class I
- Regulation Number
- 864.1850
- Review Panel
- PA
- Submission Type
- 510(k) Exempt