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CIRRUS DRUG NEBULIZER MK III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860875
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1986
Days to Decision
23 days

CIRRUS DRUG NEBULIZER MK III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860875
510(k) Type
Traditional
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1986
Days to Decision
23 days