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)

NT2000

K-Number: K972244 · 1998-02-27

ApplicantBio-Medical Research, Ltd.
Decision Date1998-02-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NT2000 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Medical Research, Ltd.. It received FDA 510(k) clearance on 1998-02-27 under 510(k) number K972244. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NT2000?

NT2000 is a medical device that received FDA 510(k) clearance on 1998-02-27. The listed applicant is Bio-Medical Research, Ltd.. The 510(k) number is K972244.

When did NT2000 receive FDA 510(k) clearance?

NT2000 received FDA 510(k) clearance on 1998-02-27, under 510(k) number K972244.

Who is the listed applicant for NT2000?

The FDA 510(k) record lists Bio-Medical Research, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NT2000?

The FDA product code for NT2000 is GZJ.

Other records listing Bio-Medical Research, Ltd. 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.

K203513SLENDERTONE Evolve Abs, Type 735K180688SLENDERTONE CoreFit Abs 8, Type 734K161974SLENDERTONE® Connect Abs, Type 570K112934NEUROTECH RECOVERYK112258NEUROTECH PLUSK103031BMR FACE

View all 30 devices →

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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.

↑