Last synced on 14 November 2025 at 11:06 pm

NEOGUIDE ENDOSCOPY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070622
510(k) Type
Traditional
Applicant
NEOGUIDE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2007
Days to Decision
161 days
Submission Type
Summary

NEOGUIDE ENDOSCOPY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070622
510(k) Type
Traditional
Applicant
NEOGUIDE SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2007
Days to Decision
161 days
Submission Type
Summary