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PREEMICARE NEBUTECH NEBULIZER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K896375
510(k) Type
Traditional
Applicant
PREEMICARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1990
Days to Decision
357 days

PREEMICARE NEBUTECH NEBULIZER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K896375
510(k) Type
Traditional
Applicant
PREEMICARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1990
Days to Decision
357 days