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FDA 510(k)

MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC

K-Number: K902976 · 1990-09-07

ApplicantMedical Consultants Intl. , Ltd.
Decision Date1990-09-07
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC 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 1990-09-07 under 510(k) number K902976. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC?

MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is Medical Consultants Intl. , Ltd.. The 510(k) number is K902976.

When did MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC receive FDA 510(k) clearance?

MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC received FDA 510(k) clearance on 1990-09-07, under 510(k) number K902976.

Who is the listed applicant for MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC?

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 MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC?

The FDA product code for MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC is GZL.

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-BK894515LISS CRANIAL STIMULATOR MODEL SBL201-MK896226LISS BODY STIMULATOR MODEL SBL501-M

Related Devices (Code: GZL)

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.

K253970Wovyn Depth ElectrodeSensomedical Labs, Ltd.K250363Depth Electrode (RSDE-08); Depth Electrode (RSDE-10); Depth Electrode (RSDE-12); Depth Electrode (RSDE-14); Depth Electrode (RSDE-16); Depth Electrode (RSDE-16F); Depth Electrode (RSDE-08S); Depth Electrode (RSDE-10S); Depth Electrode (RSDE-12S); Depth Electrode (RSDE-14S); Depth Electrode (RSDE-16S); Depth Electrode (RSDE-16G); Depth Electrode (RSDE-18); Depth Electrode (RSDE-18F); Depth Electrode (RSDE-18T); Depth Electrode (RSDE-20); Depth Electrode (RSDE-20F); DeptBeijing Sinovation Medical Technology Co., Ltd.K250601Neuro Omega System; NeuroSmart SystemAlpha Omega Engineering , Ltd.K223276Anchor Bolts as Accessories to Depth ElectrodesAd-Tech Medical Instrument CorporationK223269Spencer Probe Depth ElectrodesAd-Tech Medical Instrument CorporationK213170SENSOSEEG Depth ElectrodesSensomedical Labs, Ltd.

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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