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FDA 510(k)

PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000

K-Number: K024036 · 2002-12-20

Decision Date2002-12-20
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000 is the device name listed in this FDA 510(k) record. The listed applicant is Johari Digital Healthcare , Ltd.. It received FDA 510(k) clearance on 2002-12-20 under 510(k) number K024036. 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 PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000?

PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000 is a medical device that received FDA 510(k) clearance on 2002-12-20. The listed applicant is Johari Digital Healthcare , Ltd.. The 510(k) number is K024036.

When did PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000 receive FDA 510(k) clearance?

PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000 received FDA 510(k) clearance on 2002-12-20, under 510(k) number K024036.

Who is the listed applicant for PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000?

The FDA 510(k) record lists Johari Digital Healthcare , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000?

The FDA product code for PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000 is IPF.

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 Johari Digital Healthcare , Ltd. 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.

View all 7 devices →

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.

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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