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Snyder Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K843906SNYDER HEMOVAC WOUND DRAINAGE DEVICESNovember 5, 1984
K821321SNYDER DEBRIBEMENT SYSTEM LDP-1August 6, 1982
K800861SNYDER HEMOVAC CHEST DRAINAGE SOLUTIONMay 2, 1980
K800578SURGIVAC TMApril 16, 1980
K800577SNYDER HEMOVAC TM VENTED WOUND KITApril 16, 1980
K800543SNYDER HYSTERECTOMY Y TUBE KITApril 16, 1980
K800542100 ML SNYDER HEMOVACApril 2, 1980
K790607GREENLINE IRRIGATION TRAYSMay 11, 1979
K790420SUCTION CONNECTING TUBINGApril 23, 1979
K790606CATHETERS, GREENLINE SUCTIONApril 23, 1979
K790419YANKAUER & POODLE SUCTION INSTRUMENTSApril 23, 1979
K790254FOLEY CATHETERIZATION TRAYApril 10, 1979
K790253URINARY DRAINAGE BAGApril 10, 1979
K790272TRAY, URETHRAL CATHETERIZATIONMarch 6, 1979
K790271TRAY AND BAG, CATHETERIZATIONMarch 6, 1979
K781400HEMOVAC TUBING MATERIAL CHANGESeptember 20, 1978