Last synced on 14 November 2025 at 11:06 pm

SUBCUTANEOUS INFUSION SET

Page Type
Cleared 510(K)
510(k) Number
K932637
510(k) Type
Traditional
Applicant
DOUGLAS MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1994
Days to Decision
219 days
Submission Type
Statement

SUBCUTANEOUS INFUSION SET

Page Type
Cleared 510(K)
510(k) Number
K932637
510(k) Type
Traditional
Applicant
DOUGLAS MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1994
Days to Decision
219 days
Submission Type
Statement