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FDA 510(k)

BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE

K-Number: K863557 · 1986-10-06

ApplicantAmerican Safety Razor Co.
Decision Date1986-10-06
Product Code
DecisionSubstantially Equivalent

Device Summary

BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE is the device name listed in this FDA 510(k) record. The listed applicant is American Safety Razor Co.. It received FDA 510(k) clearance on 1986-10-06 under 510(k) number K863557. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE?

BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE is a medical device that received FDA 510(k) clearance on 1986-10-06. The listed applicant is American Safety Razor Co.. The 510(k) number is K863557.

When did BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE receive FDA 510(k) clearance?

BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE received FDA 510(k) clearance on 1986-10-06, under 510(k) number K863557.

Who is the listed applicant for BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE?

The FDA 510(k) record lists American Safety Razor Co. as the applicant. This does not by itself establish the device manufacturer.

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 American Safety Razor 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.

K924503PERSONNA SAFETY SCALPELK873142PERSONNA DISPOSABLE SCALPELK771045BLADES, SCALPEL

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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