Last synced on 6 June 2025 at 11:06 pm

REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071764
510(k) Type
Traditional
Applicant
OBTECH MEDICAL SARL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2007
Days to Decision
117 days
Submission Type
Summary

REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071764
510(k) Type
Traditional
Applicant
OBTECH MEDICAL SARL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2007
Days to Decision
117 days
Submission Type
Summary