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NEXUS PRESSURE RATED EXTENSION SETS

Page Type
Cleared 510(K)
510(k) Number
K092382
510(k) Type
Traditional
Applicant
NEXUS MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2010
Days to Decision
264 days
Submission Type
Statement

NEXUS PRESSURE RATED EXTENSION SETS

Page Type
Cleared 510(K)
510(k) Number
K092382
510(k) Type
Traditional
Applicant
NEXUS MEDICAL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2010
Days to Decision
264 days
Submission Type
Statement