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INFRA VISION BOUGIE KIT, INFRA VISION ESOPHAGEAL KIT

Page Type
Cleared 510(K)
510(k) Number
K960173
510(k) Type
Traditional
Applicant
Gabriel Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
163 days
Submission Type
Summary

INFRA VISION BOUGIE KIT, INFRA VISION ESOPHAGEAL KIT

Page Type
Cleared 510(K)
510(k) Number
K960173
510(k) Type
Traditional
Applicant
Gabriel Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1996
Days to Decision
163 days
Submission Type
Summary