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Sherwood Medical Industries

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
62
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESJuly 21, 1980
K801071LANCER GLUCOSE RATE REAGENT KITMay 23, 1980
K792013LANCER L-INA HUMAN REFERENCE SERUMNovember 13, 1979
K792014LANCER L-INA BUFFER, POLYMER, WASH SOLUNovember 13, 1979
K782077LANCER ICE CUBEApril 3, 1979
K790523ARGYLE ESOPHAGEAL STETHOSCOPEMarch 27, 1979
K790196MONOJECT ARTERIAL BLOOD SAMPLING DEVICEMarch 13, 1979
K790197REAGENT KIT, LANCER GLUCOSEMarch 12, 1979
K781459MONOJECT SCALE MAGNIFIEROctober 24, 1978
K781060MONOJECT ENDOSSEOUS DENTAL IMPLANTAugust 14, 1978
K772149LANCER BIOPSY HOLDERNovember 22, 1977
K771876ARGYLE PEOCUSSOR SYSTEMOctober 28, 1977
K771116CATHETER, PO2, INTRAVASUCLAR, CITADELSeptember 15, 1977
K770981LANCER CAPILLARY BLOOD SERUM SEPARATORJuly 11, 1977
K771055BLOOD COLLECTION TUBE, REDJune 29, 1977
K771053BLOOD COLLECTION TUBE, GRAYJune 29, 1977
K771054BLOOD COLLECTION TUBE, BLUEJune 29, 1977
K771056BLOOD COLLECTION TUBE, GREENJune 29, 1977
K771052BLOOD COLLECTION TUBE, LAVENDERJune 27, 1977
K770920THORACIC DRAINAGE SET, ARGYLE DUALJune 24, 1977