DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226
K-Number: K031697 · 2003-08-29
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Device Summary
Frequently Asked Questions
What is the DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226?
DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226 is a medical device that received FDA 510(k) clearance on 2003-08-29. The listed applicant is Schering-Plough Healthcare Products, Inc.. The 510(k) number is K031697.
When did DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226 receive FDA 510(k) clearance?
DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226 received FDA 510(k) clearance on 2003-08-29, under 510(k) number K031697.
Who is the listed applicant for DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226?
The FDA 510(k) record lists Schering-Plough Healthcare Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226?
The FDA product code for DR. SCHOLL'S FREEZE AWAY WART REMOVER, MODEL 40226 is GEH.
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 Schering-Plough Healthcare Products, 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: GEH)
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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