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FDA 510(k)

MULTI CARE THERAPEUTIC VIBRATOR

K-Number: K010096 · 2001-03-05

ApplicantMulticept A/S
Decision Date2001-03-05
Product CodeKXQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MULTI CARE THERAPEUTIC VIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Multicept A/S. It received FDA 510(k) clearance on 2001-03-05 under 510(k) number K010096. The device is classified under product code KXQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI CARE THERAPEUTIC VIBRATOR?

MULTI CARE THERAPEUTIC VIBRATOR is a medical device that received FDA 510(k) clearance on 2001-03-05. The listed applicant is Multicept A/S. The 510(k) number is K010096.

When did MULTI CARE THERAPEUTIC VIBRATOR receive FDA 510(k) clearance?

MULTI CARE THERAPEUTIC VIBRATOR received FDA 510(k) clearance on 2001-03-05, under 510(k) number K010096.

Who is the listed applicant for MULTI CARE THERAPEUTIC VIBRATOR?

The FDA 510(k) record lists Multicept A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI CARE THERAPEUTIC VIBRATOR?

The FDA product code for MULTI CARE THERAPEUTIC VIBRATOR is KXQ.

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.

Related Devices (Code: KXQ)

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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