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FDA 510(k)

MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)

K-Number: K900731 · 1990-12-17

ApplicantMedical Consultants Intl. , Ltd.
Decision Date1990-12-17
Product CodeLWM
DecisionSubstantially Equivalent

Device Summary

MEDI LISS DENTAL ANALGESIA DEVICE (SBL601) 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 1990-12-17 under 510(k) number K900731. The device is classified under product code LWM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)?

MEDI LISS DENTAL ANALGESIA DEVICE (SBL601) is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is Medical Consultants Intl. , Ltd.. The 510(k) number is K900731.

When did MEDI LISS DENTAL ANALGESIA DEVICE (SBL601) receive FDA 510(k) clearance?

MEDI LISS DENTAL ANALGESIA DEVICE (SBL601) received FDA 510(k) clearance on 1990-12-17, under 510(k) number K900731.

Who is the listed applicant for MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)?

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 LISS DENTAL ANALGESIA DEVICE (SBL601)?

The FDA product code for MEDI LISS DENTAL ANALGESIA DEVICE (SBL601) is LWM.

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 STIMULATORK903654LISS CRANIAL STIMULATOR MODEL SBL202-BK902976MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DCK894515LISS CRANIAL STIMULATOR MODEL SBL201-MK896226LISS BODY STIMULATOR MODEL SBL501-M

Related Devices (Code: LWM)

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.

K193570Dental Pain EraserSynapse DentalK192429Dental Pain EraserSynapse DentalK182947Dental Pain EraserSynapse Dental, LLCK011001TEAM-UP TM DENTAL ELECTRONIC ANESTHESIA SYSTEMSatelecK9353043M DENTAL ELECTRONIC ANESTHESIA (DEA) SYSTEM 86703M CompanyK9350853M DENTAL ELECTRONONIC ANESTHESIA (DEA0 SYSTEM 8670 ADDITIONAL APPLICATIONS3M Company

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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