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HEART NUBULIZER

Page Type
Cleared 510(K)
510(k) Number
K920332
510(k) Type
Traditional
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1992
Days to Decision
124 days
Submission Type
Statement

HEART NUBULIZER

Page Type
Cleared 510(K)
510(k) Number
K920332
510(k) Type
Traditional
Applicant
VORTRAN MEDICAL TECHNOLOGY 1, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/1992
Days to Decision
124 days
Submission Type
Statement