Esa, Inc.
Esa, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 30, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K032199 | ESA PLASMA FREE METANEPHRINE ANALYSIS KIT | January 30, 2004 |
| K971640 | LEADCARE BLOOD LEAD TESTING SYSTEM | September 9, 1997 |
| K963938 | MODEL 5500 CEAS | December 26, 1996 |
| K934977 | MODEL 5500 CEAS | January 11, 1994 |
| K931148 | MODEL 5500 COULOCHEM ELECTRODE ARRAY SYSTEM | June 9, 1993 |
| K903231 | COULOCHEM II | September 27, 1990 |
| K864729 | NEUROCHEMICAL ANALYZER | April 13, 1987 |