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FDA 510(k)

FERTICARE PERSONAL THERAPEUTIC VIBRATOR

K-Number: K955589 · 1996-04-11

ApplicantMulticept, Aps.
Decision Date1996-04-11
Product CodeKXQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FERTICARE PERSONAL THERAPEUTIC VIBRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Multicept, Aps.. It received FDA 510(k) clearance on 1996-04-11 under 510(k) number K955589. 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 FERTICARE PERSONAL THERAPEUTIC VIBRATOR?

FERTICARE PERSONAL THERAPEUTIC VIBRATOR is a medical device that received FDA 510(k) clearance on 1996-04-11. The listed applicant is Multicept, Aps.. The 510(k) number is K955589.

When did FERTICARE PERSONAL THERAPEUTIC VIBRATOR receive FDA 510(k) clearance?

FERTICARE PERSONAL THERAPEUTIC VIBRATOR received FDA 510(k) clearance on 1996-04-11, under 510(k) number K955589.

Who is the listed applicant for FERTICARE PERSONAL THERAPEUTIC VIBRATOR?

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

What is the FDA product code for FERTICARE PERSONAL THERAPEUTIC VIBRATOR?

The FDA product code for FERTICARE PERSONAL 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Multicept, Aps. 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.

K851646VIBRECTOR

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.

K110566VIBERECT PENILE VIBRATORY STIMULATION DEVICEReflexonic, LLCK010096MULTI CARE THERAPEUTIC VIBRATORMulticept A/S

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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