BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD
K-Number: K990179 · 1999-08-13
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Device Summary
Frequently Asked Questions
What is the BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD?
BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD 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 K990179.
When did BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD receive FDA 510(k) clearance?
BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD received FDA 510(k) clearance on 1999-08-13, under 510(k) number K990179.
Who is the listed applicant for BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD?
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 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD?
The FDA product code for BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD 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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