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FDA 510(k)

GALVANIC GENERATOR MODEL IMF4150/A

K-Number: K932916 · 1994-01-07

ApplicantBiomedical Life Systems, Inc.
Decision Date1994-01-07
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GALVANIC GENERATOR MODEL IMF4150/A 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 1994-01-07 under 510(k) number K932916. 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 GALVANIC GENERATOR MODEL IMF4150/A?

GALVANIC GENERATOR MODEL IMF4150/A is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Biomedical Life Systems, Inc.. The 510(k) number is K932916.

When did GALVANIC GENERATOR MODEL IMF4150/A receive FDA 510(k) clearance?

GALVANIC GENERATOR MODEL IMF4150/A received FDA 510(k) clearance on 1994-01-07, under 510(k) number K932916.

Who is the listed applicant for GALVANIC GENERATOR MODEL IMF4150/A?

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 GALVANIC GENERATOR MODEL IMF4150/A?

The FDA product code for GALVANIC GENERATOR MODEL IMF4150/A is IPF.

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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: 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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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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