Last synced on 9 May 2025 at 11:05 pm

LO-PROFILE EXTENSIONSET W/ .22 MICRON FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925430
510(k) Type
Traditional
Applicant
DOUGLAS MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1993
Days to Decision
280 days
Submission Type
Statement

LO-PROFILE EXTENSIONSET W/ .22 MICRON FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K925430
510(k) Type
Traditional
Applicant
DOUGLAS MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1993
Days to Decision
280 days
Submission Type
Statement