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MICROCIRRUS MEDICAL NEBULIZER

Page Type
Cleared 510(K)
510(k) Number
K881935
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1988
Days to Decision
44 days

MICROCIRRUS MEDICAL NEBULIZER

Page Type
Cleared 510(K)
510(k) Number
K881935
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1988
Days to Decision
44 days