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FDA 510(k)

LISS CRANIAL STIMULATOR MODEL SBL201-M

K-Number: K894515 · 1990-05-03

ApplicantMedical Consultants Intl. , Ltd.
Decision Date1990-05-03
Product CodeQJQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LISS CRANIAL STIMULATOR MODEL SBL201-M is the device name listed in this FDA 510(k) record. The listed applicant is Medical Consultants Intl. , Ltd.. It received FDA 510(k) clearance on 1990-05-03 under 510(k) number K894515. The device is classified under product code QJQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LISS CRANIAL STIMULATOR MODEL SBL201-M?

LISS CRANIAL STIMULATOR MODEL SBL201-M is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is Medical Consultants Intl. , Ltd.. The 510(k) number is K894515.

When did LISS CRANIAL STIMULATOR MODEL SBL201-M receive FDA 510(k) clearance?

LISS CRANIAL STIMULATOR MODEL SBL201-M received FDA 510(k) clearance on 1990-05-03, under 510(k) number K894515.

Who is the listed applicant for LISS CRANIAL STIMULATOR MODEL SBL201-M?

The FDA 510(k) record lists Medical Consultants Intl. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LISS CRANIAL STIMULATOR MODEL SBL201-M?

The FDA product code for LISS CRANIAL STIMULATOR MODEL SBL201-M is QJQ.

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.

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Other records listing Medical Consultants Intl. , Ltd. 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.

K904264MODEL SW-103 SOLITANS STIMULATORK900731MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)K903654LISS CRANIAL STIMULATOR MODEL SBL202-BK902976MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DCK896226LISS BODY STIMULATOR MODEL SBL501-M

Related Devices (Code: QJQ)

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.

K252951Genesis SleepNeurofield, Inc.K232253Modius StressNeurovalens LimitedK230826Modius SleepNeurovalens , Ltd.K182311CervellaInnovative Neurological Devices, LLCK090052CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/CJohari Digital Healthcare , Ltd.K070412ELEXOMA MEDICRedplane AG

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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