MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR)
K-Number: K864284 · 1986-12-29
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Device Summary
Frequently Asked Questions
What is the MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR)?
MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is Modern Systems Technology, Inc.. The 510(k) number is K864284.
When did MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) receive FDA 510(k) clearance?
MUSCLE MASTER (MEDIUM VOLTAGE STIMULATOR) received FDA 510(k) clearance on 1986-12-29, under 510(k) number K864284.
Who is the listed applicant for MUSCLE MASTER (MEDIUM VOLTAGE 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 (MEDIUM VOLTAGE STIMULATOR)?
The FDA product code for MUSCLE MASTER (MEDIUM VOLTAGE 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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