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FDA 510(k)

HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7

K-Number: K040306 · 2004-03-23

ApplicantBiomedical Life Systems, Inc.
Decision Date2004-03-23
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 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 2004-03-23 under 510(k) number K040306. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7?

HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 is a medical device that received FDA 510(k) clearance on 2004-03-23. The listed applicant is Biomedical Life Systems, Inc.. The 510(k) number is K040306.

When did HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 receive FDA 510(k) clearance?

HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 received FDA 510(k) clearance on 2004-03-23, under 510(k) number K040306.

Who is the listed applicant for HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7?

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 HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7?

The FDA product code for HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 is IPF.

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Other records listing Biomedical Life Systems, Inc. as applicant

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Related Devices (Code: IPF)

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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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