Last synced on 14 November 2025 at 11:06 pm

PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIAL

Page Type
Cleared 510(K)
510(k) Number
K890707
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
59 days

PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIAL

Page Type
Cleared 510(K)
510(k) Number
K890707
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
59 days