Last synced on 20 May 2022 at 11:05 pm

PLEXUFIX BRACHIAL PLEXUS ANESTH. NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813165
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1981
Days to Decision
23 days

PLEXUFIX BRACHIAL PLEXUS ANESTH. NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813165
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1981
Days to Decision
23 days