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Lifeline Instruments, Inc.

FDA Regulatory Profile

Lifeline Instruments, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 7, 1981.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810617MOBILE MATIC AUTOMATIC DONOR SCALEApril 7, 1981
K760743DONORMATIC (BLOOD COLLECTION DEVICE)December 6, 1976

FDA data resources