Schiff & Co.
Schiff & Co. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1999.
Top product codes for Schiff & Co.
Recent clearances by Schiff & Co.
- K990511 — X-TIP INTRAOSSEOUS PERFORATOR
- K982136 — JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200
- K981629 — NUTRISAFE ENTERAL FEEDING TUBE
- K981630 — VYGON DOUBLE LUMEN UMBILICAL CATHETER
- K974141 — PLUS REUSABLE RESUSCITATOR
- K954448 — VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM
- K955085 — HM-CAP EIA TEST (MODIFICATION)
- K944159 — HM-CAP EIA KIT
- K943521 — VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE
- K896684 — KEMBLE LIQUID HANDLING SYSTEM DISPENSER
- K894617 — OLYMPUS PK-TP SYSTEM REACTIVE CONTROL
- K895967 — FASTEC 901 AGGLUTINATION PATTERN READER
- K882539 — CLEANTECH SYSTEM
- K874482 — REVISED IMMUDIA HEM-SP
- K873986 — BETA-HCG ASSAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.