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EPIDURAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K823702
510(k) Type
Traditional
Applicant
RSP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1983
Days to Decision
29 days

EPIDURAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K823702
510(k) Type
Traditional
Applicant
RSP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1983
Days to Decision
29 days