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SPIROXCARD DIAGNOSTIC SPIROMETER AND PULSE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K001995
510(k) Type
Special
Applicant
QRS DIAGNOSTIC, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2000
Days to Decision
70 days
Submission Type
Summary

SPIROXCARD DIAGNOSTIC SPIROMETER AND PULSE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K001995
510(k) Type
Special
Applicant
QRS DIAGNOSTIC, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2000
Days to Decision
70 days
Submission Type
Summary