MYOCARE PLUS DUAL CHANNEL STIMULATOR
K-Number: K851046 · 1985-07-01
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Device Summary
Frequently Asked Questions
What is the MYOCARE PLUS DUAL CHANNEL STIMULATOR?
MYOCARE PLUS DUAL CHANNEL STIMULATOR is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is 3M Company. The 510(k) number is K851046.
When did MYOCARE PLUS DUAL CHANNEL STIMULATOR receive FDA 510(k) clearance?
MYOCARE PLUS DUAL CHANNEL STIMULATOR received FDA 510(k) clearance on 1985-07-01, under 510(k) number K851046.
Who is the listed applicant for MYOCARE PLUS DUAL CHANNEL STIMULATOR?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYOCARE PLUS DUAL CHANNEL STIMULATOR?
The FDA product code for MYOCARE PLUS DUAL CHANNEL 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 3M Company 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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