KEQ — Media, Mounting, Water Soluble Class I
FDA product code KEQ covers "Media, Mounting, Water Soluble", a Class I medical device regulated under 21 CFR 864.4010. Submissions are reviewed by the Pathology panel. At least 7 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- KEQ
- Device Class
- Class I
- Regulation Number
- 864.4010
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Pathology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K830515 | surgipath medical industries | SCOTTS TAP WATER SUBSTITUTE CONCENTRATE | March 31, 1983 |
| K792703 | meridian diagnostics | LACTO-PHENOL ANALINE BLUE FLUID | January 24, 1980 |
| K792709 | meridian diagnostics | KOH MOUNTING FLUID W/GLYCEROL | January 24, 1980 |
| K792702 | meridian diagnostics | VASPAR SEALANT | January 24, 1980 |
| K781868 | marion laboratories | DROPPER, CEPTI-SEAL LAVTOPHENOL | November 22, 1978 |
| K781869 | marion laboratories | DROPPER, CEPTI-SEAL KOH SOLUTION | November 22, 1978 |
| K781388 | flow laboratories | F.A. MOUNTING MEDIUM | August 21, 1978 |