Last synced on 14 November 2025 at 11:06 pm

PROCEDUR 10 SYRINGE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K042486
510(k) Type
Traditional
Applicant
AVANCA MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2005
Days to Decision
130 days
Submission Type
Summary

PROCEDUR 10 SYRINGE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K042486
510(k) Type
Traditional
Applicant
AVANCA MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2005
Days to Decision
130 days
Submission Type
Summary