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FDA 510(k)

OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142

K-Number: K926246 · 1993-04-14

Decision Date1993-04-14
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142 is the device name listed in this FDA 510(k) record. The listed applicant is Omron Healthcare, Inc.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K926246. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142?

OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142 is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K926246.

When did OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142 receive FDA 510(k) clearance?

OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142 received FDA 510(k) clearance on 1993-04-14, under 510(k) number K926246.

Who is the listed applicant for OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142?

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

What is the FDA product code for OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142?

The FDA product code for OMRON RECHARGEABLE PLAQUE REMOVAL SYSTEM #HT-B142 is JEQ.

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 Omron Healthcare, 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.

View all 63 devices →

Related Devices (Code: JEQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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