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FDA 510(k)

BMLS03-3

K-Number: K033174 · 2004-06-30

ApplicantBiomedical Life Systems, Inc.
Decision Date2004-06-30
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BMLS03-3 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 2004-06-30 under 510(k) number K033174. 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 BMLS03-3?

BMLS03-3 is a medical device that received FDA 510(k) clearance on 2004-06-30. The listed applicant is Biomedical Life Systems, Inc.. The 510(k) number is K033174.

When did BMLS03-3 receive FDA 510(k) clearance?

BMLS03-3 received FDA 510(k) clearance on 2004-06-30, under 510(k) number K033174.

Who is the listed applicant for BMLS03-3?

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 BMLS03-3?

The FDA product code for BMLS03-3 is IPF.

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: IPF)

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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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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