BURNFREE PAIN RELIEVING GEL, MODEL 4B
K-Number: K990178 · 1999-08-13
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Device Summary
Frequently Asked Questions
What is the BURNFREE PAIN RELIEVING GEL, MODEL 4B?
BURNFREE PAIN RELIEVING GEL, MODEL 4B is a medical device that received FDA 510(k) clearance on 1999-08-13. The listed applicant is Nortrade Medical, Inc.. The 510(k) number is K990178.
When did BURNFREE PAIN RELIEVING GEL, MODEL 4B receive FDA 510(k) clearance?
BURNFREE PAIN RELIEVING GEL, MODEL 4B received FDA 510(k) clearance on 1999-08-13, under 510(k) number K990178.
Who is the listed applicant for BURNFREE PAIN RELIEVING GEL, MODEL 4B?
The FDA 510(k) record lists Nortrade Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BURNFREE PAIN RELIEVING GEL, MODEL 4B?
The FDA product code for BURNFREE PAIN RELIEVING GEL, MODEL 4B is MGQ.
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 Nortrade 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: MGQ)
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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