Last synced on 14 November 2025 at 11:06 pm

BORDISPO BRAND HYPODERMIC NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K790953
510(k) Type
Traditional
Applicant
BORDA PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1979
Days to Decision
36 days

BORDISPO BRAND HYPODERMIC NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K790953
510(k) Type
Traditional
Applicant
BORDA PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1979
Days to Decision
36 days