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RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000

Page Type
Cleared 510(K)
510(k) Number
K001430
510(k) Type
Traditional
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2000
Days to Decision
61 days
Submission Type
Summary

RESPIRTECH PRO-O2C, MODEL 2200 AND RESPIRTECH PRO, MODEL 2000

Page Type
Cleared 510(K)
510(k) Number
K001430
510(k) Type
Traditional
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2000
Days to Decision
61 days
Submission Type
Summary