Last synced on 14 November 2025 at 11:06 pm

CPR SUTURE REMOVAL KIT

Page Type
Cleared 510(K)
510(k) Number
K960238
510(k) Type
Traditional
Applicant
CUSTOM PACK RELIABILITY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1996
Days to Decision
72 days
Submission Type
Statement

CPR SUTURE REMOVAL KIT

Page Type
Cleared 510(K)
510(k) Number
K960238
510(k) Type
Traditional
Applicant
CUSTOM PACK RELIABILITY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/1996
Days to Decision
72 days
Submission Type
Statement