Synemed, Inc.
Synemed, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 17, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K954037 | FIELD TREND | November 17, 1995 |
| K852936 | THE FIELDMASTER MODEL 275 | October 15, 1985 |
| K833274 | DERMATOLOGY HANDPIECE-OPHTH LASER | December 3, 1983 |
| K831085 | SYNEVAC VACUUM SOURCE UNIT | June 8, 1983 |
| K828585 | OPTHALAS PHOTOCOAGULATOR | January 3, 1983 |
| K822853 | MODEL 200 SQUID | October 18, 1982 |
| K813282 | SYNEVAC VACUUM CURETTAGE SYSTEMS | December 14, 1981 |
| K811270 | SCOPE MASTER | September 8, 1981 |