Snyder Laboratories, Inc.
Snyder Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1984.
Top product codes for Snyder Laboratories, Inc.
Recent clearances by Snyder Laboratories, Inc.
- K843906 — SNYDER HEMOVAC WOUND DRAINAGE DEVICES
- K821321 — SNYDER DEBRIBEMENT SYSTEM LDP-1
- K800861 — SNYDER HEMOVAC CHEST DRAINAGE SOLUTION
- K800543 — SNYDER HYSTERECTOMY Y TUBE KIT
- K800577 — SNYDER HEMOVAC TM VENTED WOUND KIT
- K800578 — SURGIVAC TM
- K800542 — 100 ML SNYDER HEMOVAC
- K790607 — GREENLINE IRRIGATION TRAYS
- K790419 — YANKAUER & POODLE SUCTION INSTRUMENTS
- K790420 — SUCTION CONNECTING TUBING
- K790606 — CATHETERS, GREENLINE SUCTION
- K790253 — URINARY DRAINAGE BAG
- K790254 — FOLEY CATHETERIZATION TRAY
- K790271 — TRAY AND BAG, CATHETERIZATION
- K790272 — TRAY, URETHRAL CATHETERIZATION
- K781400 — HEMOVAC TUBING MATERIAL CHANGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.