STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ
K-Number: K940600 · 1995-09-29
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Device Summary
Frequently Asked Questions
What is the STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ?
STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Progressive Concepts, Inc.. The 510(k) number is K940600.
When did STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ receive FDA 510(k) clearance?
STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ received FDA 510(k) clearance on 1995-09-29, under 510(k) number K940600.
Who is the listed applicant for STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ?
The FDA 510(k) record lists Progressive Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ?
The FDA product code for STIMULATOR, NERVE, TRANSCUTANEOUS, (PAIN RELIEF) 84-GZJ 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 Progressive Concepts, 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: 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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