FDA 510(k)

PERSONNA SAFETY SCALPEL

K-Number: K924503 · 1993-02-05

Decision Date1993-02-05

Product CodeMDM

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PERSONNA SAFETY SCALPEL 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 1993-02-05 under 510(k) number K924503. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERSONNA SAFETY SCALPEL?

PERSONNA SAFETY SCALPEL is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is American Safety Razor Co.. The 510(k) number is K924503.

When did PERSONNA SAFETY SCALPEL receive FDA 510(k) clearance?

PERSONNA SAFETY SCALPEL received FDA 510(k) clearance on 1993-02-05, under 510(k) number K924503.

Who is the listed applicant for PERSONNA SAFETY SCALPEL?

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

What is the FDA product code for PERSONNA SAFETY SCALPEL?

The FDA product code for PERSONNA SAFETY SCALPEL is MDM.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing American Safety Razor Co. as applicant

K873142PERSONNA DISPOSABLE SCALPEL K863557BLADE, SURGICAL PREPARATION RAZOR, STRAIGHT,SINGLE K771045BLADES, SCALPEL

Related Devices (Code: MDM)

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn Bhd K050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific Corp K013040LIGHT SABER INTRODUCER NEEDLEMinrad, Inc.

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.