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FDA 510(k)

OMRON PULSE STIMULATOR MODEL HV-F05

K-Number: K902255 · 1990-10-31

ApplicantOmron Electronics, Inc.
Decision Date1990-10-31
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OMRON PULSE STIMULATOR MODEL HV-F05 is the device name listed in this FDA 510(k) record. The listed applicant is Omron Electronics, Inc.. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K902255. 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 OMRON PULSE STIMULATOR MODEL HV-F05?

OMRON PULSE STIMULATOR MODEL HV-F05 is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Omron Electronics, Inc.. The 510(k) number is K902255.

When did OMRON PULSE STIMULATOR MODEL HV-F05 receive FDA 510(k) clearance?

OMRON PULSE STIMULATOR MODEL HV-F05 received FDA 510(k) clearance on 1990-10-31, under 510(k) number K902255.

Who is the listed applicant for OMRON PULSE STIMULATOR MODEL HV-F05?

The FDA 510(k) record lists Omron Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OMRON PULSE STIMULATOR MODEL HV-F05?

The FDA product code for OMRON PULSE STIMULATOR MODEL HV-F05 is IPF.

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Other records listing Omron Electronics, Inc. as applicant

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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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