ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3
K-Number: K021271 · 2003-02-06
Advertisement
Device Summary
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.
Advertisement