Schiff & Co.
Schiff & Co. appears in FDA public data with 0 recalls, 15 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 27, 1999.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 15
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K990511 | X-TIP INTRAOSSEOUS PERFORATOR | April 27, 1999 |
| K982136 | JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 | March 24, 1999 |
| K981629 | NUTRISAFE ENTERAL FEEDING TUBE | February 4, 1999 |
| K981630 | VYGON DOUBLE LUMEN UMBILICAL CATHETER | October 1, 1998 |
| K974141 | PLUS REUSABLE RESUSCITATOR | May 21, 1998 |
| K954448 | VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM | October 28, 1996 |
| K955085 | HM-CAP EIA TEST (MODIFICATION) | February 9, 1996 |
| K944159 | HM-CAP EIA KIT | July 18, 1995 |
| K943521 | VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE | February 14, 1995 |
| K896684 | KEMBLE LIQUID HANDLING SYSTEM DISPENSER | April 16, 1990 |
| K894617 | OLYMPUS PK-TP SYSTEM REACTIVE CONTROL | October 31, 1989 |
| K895967 | FASTEC 901 AGGLUTINATION PATTERN READER | October 30, 1989 |
| K882539 | CLEANTECH SYSTEM | August 8, 1988 |
| K874482 | REVISED IMMUDIA HEM-SP | May 13, 1988 |
| K873986 | BETA-HCG ASSAY | February 2, 1988 |