Hirata Sangyo Co. USA, Inc.
Hirata Sangyo Co. USA, 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 Nov 19, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K864106 | SR-MODEL 230 (MODIFICATION) | Nov 19, 1986 |
| K842289 | SR- MODEL 230 | Jul 25, 1984 |
| K833541 | SURGICAL INSTRUMENT | Nov 28, 1983 |
| K833542 | SURGICAL INSTRUMENT | Nov 28, 1983 |
| K832686 | MULTIPLE MANUAL SURGICAL INSTRUMENTS | Oct 14, 1983 |
| K831583 | GP-303 | Jul 19, 1983 |
| K821989 | NON-STETHO 7, UM-15TP | Oct 18, 1982 |
| K822571 | SYRINGE PUMP | Oct 8, 1982 |