I M, Inc.

FDA Regulatory Profile

I M, Inc. appears in FDA public data with 0 recalls, 41 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 30, 1992.

Summary

Total Recalls
0
510(k) Clearances
41
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K914600NEUROLOGICAL SPONGEDecember 30, 1992
K892389BIOPSY KITJuly 17, 1989
K881363SYRINGE PREFILLED WITH WATERJune 23, 1988
K880753UMBILICAL CORD CLAMPApril 27, 1988
K872741NUTRIPUMPOctober 20, 1987
K871495BANDAGES CATALOG NUMBER: 101 TO 220May 8, 1987
K863785MAKLER CATHETERDecember 11, 1986
K854155STERILE SALINE SOLUTIONDecember 10, 1985
K853287HUBOUTOctober 17, 1985
K853288FEEDING UNITS & TUBESOctober 4, 1985
K853286STAPLE REMOVERAugust 21, 1985
K844062FORCEPS & HAMOSTATSJanuary 18, 1985
K844063SCISSORS GENERAL HOSPITALNovember 19, 1984
K844151SETS AND TRAYSNovember 7, 1984
K844152HEMSTATSNovember 7, 1984
K833399SYRINGEJanuary 10, 1984
K833435MULTI PURPOSE SYRINGEDecember 12, 1983
K831795FIRST AID KITSSeptember 1, 1983
K831794SETS & TRAYSAugust 16, 1983
K831796URINE BAG SYSTEMAugust 8, 1983