Last synced on 14 November 2025 at 11:06 pm

NEBULIZER (DIRECT PATIENT INTERFACE)

Page Type
Cleared 510(K)
510(k) Number
K915075
510(k) Type
Traditional
Applicant
MEDI NUCLEAR CORP., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1992
Days to Decision
251 days
Submission Type
Statement

NEBULIZER (DIRECT PATIENT INTERFACE)

Page Type
Cleared 510(K)
510(k) Number
K915075
510(k) Type
Traditional
Applicant
MEDI NUCLEAR CORP., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1992
Days to Decision
251 days
Submission Type
Statement