Last synced on 14 November 2025 at 11:06 pm

SINGLE WALL INTRODUCER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K843719
510(k) Type
Traditional
Applicant
OCEAN MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1984
Days to Decision
24 days

SINGLE WALL INTRODUCER NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K843719
510(k) Type
Traditional
Applicant
OCEAN MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1984
Days to Decision
24 days