STERIKING, SEE & PEEL
K-Number: K922440 · 1994-09-26
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Device Summary
Frequently Asked Questions
What is the STERIKING, SEE & PEEL?
STERIKING, SEE & PEEL is a medical device that received FDA 510(k) clearance on 1994-09-26. The listed applicant is Cox Sterile Products, Inc.. The 510(k) number is K922440.
When did STERIKING, SEE & PEEL receive FDA 510(k) clearance?
STERIKING, SEE & PEEL received FDA 510(k) clearance on 1994-09-26, under 510(k) number K922440.
Who is the listed applicant for STERIKING, SEE & PEEL?
The FDA 510(k) record lists Cox Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERIKING, SEE & PEEL?
The FDA product code for STERIKING, SEE & PEEL is KCT.
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 Cox Sterile 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: KCT)
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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