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BURRON CENTRAL VEIN CATHERIZATION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810461
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1981
Days to Decision
19 days

BURRON CENTRAL VEIN CATHERIZATION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810461
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1981
Days to Decision
19 days