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AIR PLUS NEBULIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902520
510(k) Type
Traditional
Applicant
DIAMOND MEDICAL EQUIPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1991
Days to Decision
270 days

AIR PLUS NEBULIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902520
510(k) Type
Traditional
Applicant
DIAMOND MEDICAL EQUIPMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1991
Days to Decision
270 days