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FDA 510(k)

RICH-MAR MODEL 25 ULTRASOUND

K-Number: K912202 · 1991-09-17

ApplicantRich-Mar Corp.
Decision Date1991-09-17
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RICH-MAR MODEL 25 ULTRASOUND is the device name listed in this FDA 510(k) record. The listed applicant is Rich-Mar Corp.. It received FDA 510(k) clearance on 1991-09-17 under 510(k) number K912202. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICH-MAR MODEL 25 ULTRASOUND?

RICH-MAR MODEL 25 ULTRASOUND is a medical device that received FDA 510(k) clearance on 1991-09-17. The listed applicant is Rich-Mar Corp.. The 510(k) number is K912202.

When did RICH-MAR MODEL 25 ULTRASOUND receive FDA 510(k) clearance?

RICH-MAR MODEL 25 ULTRASOUND received FDA 510(k) clearance on 1991-09-17, under 510(k) number K912202.

Who is the listed applicant for RICH-MAR MODEL 25 ULTRASOUND?

The FDA 510(k) record lists Rich-Mar Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RICH-MAR MODEL 25 ULTRASOUND?

The FDA product code for RICH-MAR MODEL 25 ULTRASOUND is IMI.

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Other records listing Rich-Mar Corp. 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.

K040679RICH-MAR AUTOPRISM INFRARED LAMPK031018AUTOGEL PADK032941AUTOSOUND 7.6 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICEK021483RICH-MAR THERASOUND 6.5 THERAPEUTIC ULTRASOUNDK013770MODIFICATION TO: WINNER ST-2 STIMULATORK013771MODIFICATION TO: WINNER CM-2 MUSCLE STIMULATOR, TENS, THERAPEUTIC ULTRASOUND AND COMBINATION DEVICE

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Related Devices (Code: IMI)

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.

K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , Ltd.

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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