FDA Product Code
FDA Product Code KEQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Pathology
- 21 CFR Citation
- 864.4010
510(k) Clearances — 7 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K830515 | SCOTTS TAP WATER SUBSTITUTE CONCENTRATE | Surgipath Medical Industries, Inc. | 1983-03-31 | Traditional | PDF ↗ |
| K792703 | LACTO-PHENOL ANALINE BLUE FLUID | Meridian Diagnostics, Inc. | 1980-01-24 | Traditional | PDF ↗ |
| K792709 | KOH MOUNTING FLUID W/GLYCEROL | Meridian Diagnostics, Inc. | 1980-01-24 | Traditional | PDF ↗ |
| K792702 | VASPAR SEALANT | Meridian Diagnostics, Inc. | 1980-01-24 | Traditional | PDF ↗ |
| K781868 | DROPPER, CEPTI-SEAL LAVTOPHENOL | Marion Laboratories, Inc. | 1978-11-22 | Traditional | PDF ↗ |
| K781869 | DROPPER, CEPTI-SEAL KOH SOLUTION | Marion Laboratories, Inc. | 1978-11-22 | Traditional | PDF ↗ |
| K781388 | F.A. MOUNTING MEDIUM | Flow Laboratories, Inc. | 1978-08-21 | Traditional | PDF ↗ |
Product code KEQ · Class I · Pathology. Data: openFDA.