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QUINTON MEDTRACK CR PLUS TREADMILL

Page Type
Cleared 510(K)
510(k) Number
K990866
510(k) Type
Traditional
Applicant
Quinton, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1999
Days to Decision
44 days
Submission Type
Statement

QUINTON MEDTRACK CR PLUS TREADMILL

Page Type
Cleared 510(K)
510(k) Number
K990866
510(k) Type
Traditional
Applicant
Quinton, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1999
Days to Decision
44 days
Submission Type
Statement