Engineering, Inc.
FDA Regulatory Profile
Engineering, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 31, 1988.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K881521 | MODIFIED SERVO SYRINGE | May 31, 1988 |
| K862749 | LS9000 SUCTION BIOPSY NEEDLE | September 15, 1986 |
| K862476 | LS3000 CANNULA UTERINE SUCTION | July 18, 1986 |
| K854359 | LM2000A SURGICAL SUCTION MONITOR | March 3, 1986 |
| K854844 | LS1000 SURGICAL ASPIRATOR II | February 12, 1986 |