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FDA 510(k)

KNOTT NG TUBE

K-Number: K971354 · 1997-11-19

ApplicantMichael M. Knott, M.D.
Decision Date1997-11-19
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KNOTT NG TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Michael M. Knott, M.D.. It received FDA 510(k) clearance on 1997-11-19 under 510(k) number K971354. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNOTT NG TUBE?

KNOTT NG TUBE is a medical device that received FDA 510(k) clearance on 1997-11-19. The listed applicant is Michael M. Knott, M.D.. The 510(k) number is K971354.

When did KNOTT NG TUBE receive FDA 510(k) clearance?

KNOTT NG TUBE received FDA 510(k) clearance on 1997-11-19, under 510(k) number K971354.

Who is the listed applicant for KNOTT NG TUBE?

The FDA 510(k) record lists Michael M. Knott, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KNOTT NG TUBE?

The FDA product code for KNOTT NG TUBE is FEG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Michael M. Knott, M.D. 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.

K981966NOSEBLEED NOSECLIP

Related Devices (Code: FEG)

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.

K17161914Fr Colon Decompression Set, Macon Colon Decompression SetCook Ireland, Ltd.K132314MEDLINE ANTI-REFLUX VALVEMedline Industries, Inc.K053410GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTORKendallK040388NEXT GENERATION SALEM SUMPKendallK960176DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTERC.R. Bard, Inc.K926073ULTRAVAC-NG(TM) NASOGASTRIC SUMP SUCTION TUBESurgimark, Inc.

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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