MUSCLE MASTER (BIPOLAR STIMULATOR)
K-Number: K862685 · 1986-11-25
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Device Summary
Frequently Asked Questions
What is the MUSCLE MASTER (BIPOLAR STIMULATOR)?
MUSCLE MASTER (BIPOLAR STIMULATOR) is a medical device that received FDA 510(k) clearance on 1986-11-25. The listed applicant is Modern Systems Technology, Inc.. The 510(k) number is K862685.
When did MUSCLE MASTER (BIPOLAR STIMULATOR) receive FDA 510(k) clearance?
MUSCLE MASTER (BIPOLAR STIMULATOR) received FDA 510(k) clearance on 1986-11-25, under 510(k) number K862685.
Who is the listed applicant for MUSCLE MASTER (BIPOLAR STIMULATOR)?
The FDA 510(k) record lists Modern Systems Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUSCLE MASTER (BIPOLAR STIMULATOR)?
The FDA product code for MUSCLE MASTER (BIPOLAR STIMULATOR) is IPF.
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 Modern Systems Technology, Inc. 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: IPF)
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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