Last synced on 14 November 2025 at 11:06 pm

AEROQUIP SAFESTART IV CATHETER

Page Type
Cleared 510(K)
510(k) Number
K970669
510(k) Type
Traditional
Applicant
AEROQUIP MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
158 days
Submission Type
Summary

AEROQUIP SAFESTART IV CATHETER

Page Type
Cleared 510(K)
510(k) Number
K970669
510(k) Type
Traditional
Applicant
AEROQUIP MEDICAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
158 days
Submission Type
Summary