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FDA 510(k)

MODEL BMLS03-7

K-Number: K042711 · 2005-03-14

ApplicantBiomedical Life Systems, Inc.
Decision Date2005-03-14
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL BMLS03-7 is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Life Systems, Inc.. It received FDA 510(k) clearance on 2005-03-14 under 510(k) number K042711. 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 MODEL BMLS03-7?

MODEL BMLS03-7 is a medical device that received FDA 510(k) clearance on 2005-03-14. The listed applicant is Biomedical Life Systems, Inc.. The 510(k) number is K042711.

When did MODEL BMLS03-7 receive FDA 510(k) clearance?

MODEL BMLS03-7 received FDA 510(k) clearance on 2005-03-14, under 510(k) number K042711.

Who is the listed applicant for MODEL BMLS03-7?

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

What is the FDA product code for MODEL BMLS03-7?

The FDA product code for MODEL BMLS03-7 is GZJ.

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Other records listing Biomedical Life Systems, 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.

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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.

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