Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TUBING, NONINVASIVE

K-Number: K945978 · 1995-01-11

Decision Date1995-01-11
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUBING, NONINVASIVE is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopic Technologies, Inc.. It received FDA 510(k) clearance on 1995-01-11 under 510(k) number K945978. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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.

↑