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)

ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3

K-Number: K021271 · 2003-02-06

Decision Date2003-02-06
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3 is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Life Systems. It received FDA 510(k) clearance on 2003-02-06 under 510(k) number K021271. 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 ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3?

ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3 is a medical device that received FDA 510(k) clearance on 2003-02-06. The listed applicant is Biomedical Life Systems. The 510(k) number is K021271.

When did ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3 receive FDA 510(k) clearance?

ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3 received FDA 510(k) clearance on 2003-02-06, under 510(k) number K021271.

Who is the listed applicant for ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3?

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

What is the FDA product code for ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3?

The FDA product code for ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3 is GZJ.

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 Biomedical Life Systems 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.

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.

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.

↑