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E. R. Squibb & Sons, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
32
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K821494RIA STAT 16June 3, 1982
K820616ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAYMarch 26, 1982
K820340T3 UPTAKE-SQUIBB DIAGNOSTIC KITMarch 4, 1982
K820341CORTISOL-SQUIBB RADIOIMMUNOASSAY KITMarch 4, 1982
K811240SUR-FIT LOOP OSTOMY O.R. SETJune 16, 1981
K811239SUR-FIT DISPOSABLE CONVEX INSERTJune 9, 1981
K811160SUR-FIT IRRIGATION SLEEVEJune 2, 1981
K811163SUR-FIT DISPOSABLE FANGE CAPMay 21, 1981
K810966DIAGOXIN SQUIBB RADIOIMMUNOASSAY KITApril 21, 1981
K810211T3 RIA KITFebruary 10, 1981
K803100STOMAHESIVE PASTE PROTECTIVE SKIN BARRJanuary 8, 1981
K802883T3-SQUIBB RIA KITDecember 19, 1980
K802456T4-SQUIBB RIA KITOctober 31, 1980
K802455ESTRIOL-SQUIBB RIA KITOctober 31, 1980
K802173URIHESIVE STRIPSSeptember 26, 1980
K802172URIHESIVE SYSTEMSeptember 26, 1980
K801703SUR-FIT SYSTEM STERILE O.R. SETSSeptember 9, 1980
K801702SUR-FIT SYSTEM PRE-OPERATION SETAugust 27, 1980
K800997DIGOXIN CLASP RIA KITMay 8, 1980
K800495SUR-FIT UROSTOMY POUCH & URINARY BAGApril 8, 1980