EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR
K-Number: K935590 · 1994-05-05
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Device Summary
Frequently Asked Questions
What is the EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR?
EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR is a medical device that received FDA 510(k) clearance on 1994-05-05. The listed applicant is Ep Medical, Inc.. The 510(k) number is K935590.
When did EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR receive FDA 510(k) clearance?
EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR received FDA 510(k) clearance on 1994-05-05, under 510(k) number K935590.
Who is the listed applicant for EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR?
The FDA 510(k) record lists Ep Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR?
The FDA product code for EP MEDICAL, INC. EP-3 CLINICAL STIMULATOR is JOQ.
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 Ep Medical, 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: JOQ)
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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