LISS BODY STIMULATOR MODEL SBL501-M
K-Number: K896226 · 1990-04-10
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Device Summary
Frequently Asked Questions
What is the LISS BODY STIMULATOR MODEL SBL501-M?
LISS BODY STIMULATOR MODEL SBL501-M is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Medical Consultants Intl. , Ltd.. The 510(k) number is K896226.
When did LISS BODY STIMULATOR MODEL SBL501-M receive FDA 510(k) clearance?
LISS BODY STIMULATOR MODEL SBL501-M received FDA 510(k) clearance on 1990-04-10, under 510(k) number K896226.
Who is the listed applicant for LISS BODY STIMULATOR MODEL SBL501-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 BODY STIMULATOR MODEL SBL501-M?
The FDA product code for LISS BODY STIMULATOR MODEL SBL501-M is GZJ.
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.
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.
Related Devices (Code: GZJ)
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.
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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