REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360
K-Number: K071764 · 2007-10-24
Advertisement
Device Summary
Frequently Asked Questions
What is the REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360?
REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360 is a medical device that received FDA 510(k) clearance on 2007-10-24. The listed applicant is Obtech Medical Sarl. The 510(k) number is K071764.
When did REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360 receive FDA 510(k) clearance?
REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360 received FDA 510(k) clearance on 2007-10-24, under 510(k) number K071764.
Who is the listed applicant for REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360?
The FDA 510(k) record lists Obtech Medical Sarl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360?
The FDA product code for REALIZE GASTRIC CALIBRATION TUBE, MODELS GCT180, GCT360 is KNT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KNT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement