Last synced on 14 November 2025 at 11:06 pm

MULTI-CENTRIFUGE

Page Type
Cleared 510(K)
510(k) Number
K955795
510(k) Type
Traditional
Applicant
Novonx, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1996
Days to Decision
98 days
Submission Type
Summary

MULTI-CENTRIFUGE

Page Type
Cleared 510(K)
510(k) Number
K955795
510(k) Type
Traditional
Applicant
Novonx, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1996
Days to Decision
98 days
Submission Type
Summary