Symbiosis Corp.
Symbiosis Corp. appears in FDA public data with 0 recalls, 34 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 18, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 34
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K955119 | SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES | January 18, 1996 |
| K953453 | SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES | January 17, 1996 |
| K953242 | SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES | October 6, 1995 |
| K952432 | SYMBIOSIS BIPOLAR FORCEPS | July 5, 1995 |
| K951387 | SYMBIOSIS BIPOLAR SCISSORS | April 10, 1995 |
| K950286 | SYMBIOSIS BIPOLAR SCISSORS | February 3, 1995 |
| K946238 | SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS | January 20, 1995 |
| K930773 | SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS | July 28, 1994 |
| K941426 | SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE | June 22, 1994 |
| K932266 | SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN | March 15, 1994 |
| K931957 | SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS | February 28, 1994 |
| K924016 | SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST. | December 6, 1993 |
| K932265 | SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND | August 9, 1993 |
| K931793 | SYMBIOSIS ENT SURGICAL INSTRUMENTS | July 22, 1993 |
| K930160 | ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE | July 6, 1993 |
| K930158 | BONE MARROW BIOPSY PROCEDURE TRAY | July 2, 1993 |
| K926109 | FLUID DRAINAGE TRAY | June 7, 1993 |
| K925707 | INSTRUMENT, MANUAL, GENERAL SURGICAL | May 26, 1993 |
| K924501 | GILLAM-TUKEL BONE MARROW BIOPSY NEEDLE | April 20, 1993 |
| K924017 | SYMBIOSIS DISPOSABLE ARTHROSCOPIC SURGICAL INST. | March 16, 1993 |