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Fitness Quest, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K921444
DIGI SPORTLENS SYSTEM
July 13, 1992
K914595
PULSE RATE MONITOR
January 31, 1992