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SPINOCAN SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K820047
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1982
Days to Decision
17 days

SPINOCAN SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K820047
510(k) Type
Traditional
Applicant
BURRON MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1982
Days to Decision
17 days