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FDA 510(k)

VIBRECTOR

K-Number: K851646 · 1985-08-21

ApplicantMulticept, Aps.
Decision Date1985-08-21
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

VIBRECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Multicept, Aps.. It received FDA 510(k) clearance on 1985-08-21 under 510(k) number K851646. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBRECTOR?

VIBRECTOR is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is Multicept, Aps.. The 510(k) number is K851646.

When did VIBRECTOR receive FDA 510(k) clearance?

VIBRECTOR received FDA 510(k) clearance on 1985-08-21, under 510(k) number K851646.

Who is the listed applicant for VIBRECTOR?

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 VIBRECTOR?

The FDA product code for VIBRECTOR is LIL.

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.

K955589FERTICARE PERSONAL THERAPEUTIC VIBRATOR

Related Devices (Code: LIL)

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.

K061676RIGIDOMETER, MODEL DIR-4UUroan 21K062042PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)Plethora SolutionsK052929PREFTEST PROFESSIONAL SUITELimestone Technologies, Inc.K033126MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEMBehavioral Technology, Inc.K000194DIGITAL INFLECTION RIGIDOMETER (DIR)Uroan Xxi ElectromedicinaK991479VISER PENILE TUMESCENCE MONITORLaborie Medical Tech Corp.

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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