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FDA 510(k)

SONO 5

K-Number: K952536 · 1996-03-05

ApplicantZimmer Elektromedizin GmbH
Decision Date1996-03-05
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

SONO 5 is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Elektromedizin GmbH. It received FDA 510(k) clearance on 1996-03-05 under 510(k) number K952536. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SONO 5?

SONO 5 is a medical device that received FDA 510(k) clearance on 1996-03-05. The listed applicant is Zimmer Elektromedizin GmbH. The 510(k) number is K952536.

When did SONO 5 receive FDA 510(k) clearance?

SONO 5 received FDA 510(k) clearance on 1996-03-05, under 510(k) number K952536.

Who is the listed applicant for SONO 5?

The FDA 510(k) record lists Zimmer Elektromedizin GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONO 5?

The FDA product code for SONO 5 is IMI.

Other records listing Zimmer Elektromedizin GmbH 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.

K080735CRYOMINIK060395CRYO, MODEL V6.0K040727CRYO 5K960969GALVA 5-TK954411GALVA-5-MK924473DISPOSABLE THERAPY ELECTRODE

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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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