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FDA 510(k)

SURGICAL PREP RAZOR

K-Number: K874370 · 1987-11-13

ApplicantDerma-Safe Co.
Decision Date1987-11-13
Product CodeLWK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL PREP RAZOR is the device name listed in this FDA 510(k) record. The listed applicant is Derma-Safe Co.. It received FDA 510(k) clearance on 1987-11-13 under 510(k) number K874370. The device is classified under product code LWK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL PREP RAZOR?

SURGICAL PREP RAZOR is a medical device that received FDA 510(k) clearance on 1987-11-13. The listed applicant is Derma-Safe Co.. The 510(k) number is K874370.

When did SURGICAL PREP RAZOR receive FDA 510(k) clearance?

SURGICAL PREP RAZOR received FDA 510(k) clearance on 1987-11-13, under 510(k) number K874370.

Who is the listed applicant for SURGICAL PREP RAZOR?

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?

The FDA product code for SURGICAL PREP RAZOR 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K874234SURGICAL PREP RAZOR, STRAIGHT TYPE

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.

K9461623M(TM) SURGICAL SLIPPER, 9660 SERIESWahl Clipper Corp.K910524SURGICAL CLIPPERBaxter Healthcare CorpK874234SURGICAL PREP RAZOR, STRAIGHT TYPEDerma-Safe Co.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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