ECOGEL 300 TENS GEL
K-Number: K962681 · 1996-10-04
Advertisement
Device Summary
Frequently Asked Questions
What is the ECOGEL 300 TENS GEL?
ECOGEL 300 TENS GEL is a medical device that received FDA 510(k) clearance on 1996-10-04. The listed applicant is Eco-Med Pharmaceuticals, Inc.. The 510(k) number is K962681.
When did ECOGEL 300 TENS GEL receive FDA 510(k) clearance?
ECOGEL 300 TENS GEL received FDA 510(k) clearance on 1996-10-04, under 510(k) number K962681.
Who is the listed applicant for ECOGEL 300 TENS GEL?
The FDA 510(k) record lists Eco-Med Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ECOGEL 300 TENS GEL?
The FDA product code for ECOGEL 300 TENS GEL is GYB.
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 Eco-Med Pharmaceuticals, 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: GYB)
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.
Advertisement