Cardiac Resucitator Corp.

FDA Regulatory Profile

Cardiac Resucitator Corp. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 12, 1988.

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K882513MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORJuly 12, 1988
K871538STAT-PAD (TM)June 24, 1987
K871971MODIFIED PACE*AID MODEL 53June 24, 1987
K871569MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORJune 8, 1987
K870622HEART*AID 1000April 10, 1987
K850596PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &March 6, 1985
K850170HEART AID MODEL 97February 14, 1985
K844811PACE AID MODEL 53January 24, 1985
K843547PACE *AID MODEL 52December 17, 1984
K843358HEART-AID MODEL 80November 19, 1984
K841556HEART - AID ALS, 95July 19, 1984
K821152HEART AID #90August 6, 1982
K820507PACE* AID MODEL 50August 6, 1982
K821673HEART*AID, ALS, MODEL 95August 6, 1982
K820609HEART *AID, #80August 6, 1982
K813553PACE *AIDJanuary 18, 1982
K811028PACE AIDApril 16, 1981