SURGICAL PREP RAZOR, STRAIGHT TYPE
K-Number: K874234 · 1987-11-02
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Device Summary
Frequently Asked Questions
What is the SURGICAL PREP RAZOR, STRAIGHT TYPE?
SURGICAL PREP RAZOR, STRAIGHT TYPE is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Derma-Safe Co.. The 510(k) number is K874234.
When did SURGICAL PREP RAZOR, STRAIGHT TYPE receive FDA 510(k) clearance?
SURGICAL PREP RAZOR, STRAIGHT TYPE received FDA 510(k) clearance on 1987-11-02, under 510(k) number K874234.
Who is the listed applicant for SURGICAL PREP RAZOR, STRAIGHT TYPE?
The FDA 510(k) record lists Derma-Safe Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGICAL PREP RAZOR, STRAIGHT TYPE?
The FDA product code for SURGICAL PREP RAZOR, STRAIGHT TYPE is LWK.
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 Derma-Safe Co. 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: LWK)
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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