TUBING, NONINVASIVE
K-Number: K945978 · 1995-01-11
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Device Summary
Frequently Asked Questions
What is the TUBING, NONINVASIVE?
TUBING, NONINVASIVE is a medical device that received FDA 510(k) clearance on 1995-01-11. The listed applicant is Endoscopic Technologies, Inc.. The 510(k) number is K945978.
When did TUBING, NONINVASIVE receive FDA 510(k) clearance?
TUBING, NONINVASIVE received FDA 510(k) clearance on 1995-01-11, under 510(k) number K945978.
Who is the listed applicant for TUBING, NONINVASIVE?
The FDA 510(k) record lists Endoscopic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBING, NONINVASIVE?
The FDA product code for TUBING, NONINVASIVE is GAZ.
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.
Other records listing Endoscopic Technologies, Inc. as applicant
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: GAZ)
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.
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