Gyneco, Inc.
Gyneco, 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 5, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K861409 | SYNCARE TEMPORARY CARDIAC PACING WIRE | May 5, 1986 |
| K853216 | MASTER ENDOMET BIOPSY KIT W/PLAS CURE 3,4MM-4003,4 | April 2, 1986 |
| K852357 | GYNE-SHEAR CERVICAL BIOPSY INSTRUMENT W/DISPIS TIP | July 5, 1985 |
| K843941 | ENDOCYTE | February 25, 1985 |
| K841275 | FINE NEEDLE ASPIRATION DEVICE | August 17, 1984 |