Spectricept Skin and Wound Cleanser
K-Number: K243875 · 2025-04-21
Device Summary
Frequently Asked Questions
What is the Spectricept Skin and Wound Cleanser?
Spectricept Skin and Wound Cleanser is a medical device that received FDA 510(k) clearance on 2025-04-21. The listed applicant is Spectrum Antimicrobials, Inc.. The 510(k) number is K243875.
When did Spectricept Skin and Wound Cleanser receive FDA 510(k) clearance?
Spectricept Skin and Wound Cleanser received FDA 510(k) clearance on 2025-04-21, under 510(k) number K243875.
Who is the listed applicant for Spectricept Skin and Wound Cleanser?
The FDA 510(k) record lists Spectrum Antimicrobials, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spectricept Skin and Wound Cleanser?
The FDA product code for Spectricept Skin and Wound Cleanser is FRO. This falls under the Anesthesiology category.
Related Devices (Code: FRO)
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.