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FDA 510(k)

MOSS TUBES, INC. NASAL TUBE - MARK IV

K-Number: K984629 · 1999-03-02

ApplicantMoss Tubes, Inc.
Decision Date1999-03-02
Product CodeBSS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOSS TUBES, INC. NASAL TUBE - MARK IV is the device name listed in this FDA 510(k) record. The listed applicant is Moss Tubes, Inc.. It received FDA 510(k) clearance on 1999-03-02 under 510(k) number K984629. The device is classified under product code BSS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOSS TUBES, INC. NASAL TUBE - MARK IV?

MOSS TUBES, INC. NASAL TUBE - MARK IV is a medical device that received FDA 510(k) clearance on 1999-03-02. The listed applicant is Moss Tubes, Inc.. The 510(k) number is K984629.

When did MOSS TUBES, INC. NASAL TUBE - MARK IV receive FDA 510(k) clearance?

MOSS TUBES, INC. NASAL TUBE - MARK IV received FDA 510(k) clearance on 1999-03-02, under 510(k) number K984629.

Who is the listed applicant for MOSS TUBES, INC. NASAL TUBE - MARK IV?

The FDA 510(k) record lists Moss Tubes, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOSS TUBES, INC. NASAL TUBE - MARK IV?

The FDA product code for MOSS TUBES, INC. NASAL TUBE - MARK IV is BSS.

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 Moss Tubes, 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.

K190414Moss Gastrostomy Tube, Moss Nasal Tube – Mark IVK990389MOSS GASTROSTOMY TUBEK984628MODIFICATION OF MOSS P.E.G. TRAYK984310MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE

Related Devices (Code: BSS)

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.

K051480ENTERAL FEEDING TUBEBiosearch Medical Products, Inc.K961711ASPISAFE GASTRIC TUBEB.Braun Medical, Inc.K933596GASTRIC, CATHETER, IRRIGATION & ASPIRATIONPolamedco, Inc.K930510RADIUS ENTERAL FEEDING TUBERadius Intl., Inc.K935688AN-10S ANDERSEN TUBE WITH STYLETH.W. Andersen Products, Inc.K934348TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FRTri-Med Specialties, 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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