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FDA 510(k)

LANCE BLADES & SCALPELS

K-Number: K844001 · 1984-11-08

ApplicantPerry, Div.
Decision Date1984-11-08
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LANCE BLADES & SCALPELS is the device name listed in this FDA 510(k) record. The listed applicant is Perry, Div.. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K844001. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCE BLADES & SCALPELS?

LANCE BLADES & SCALPELS is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Perry, Div.. The 510(k) number is K844001.

When did LANCE BLADES & SCALPELS receive FDA 510(k) clearance?

LANCE BLADES & SCALPELS received FDA 510(k) clearance on 1984-11-08, under 510(k) number K844001.

Who is the listed applicant for LANCE BLADES & SCALPELS?

The FDA 510(k) record lists Perry, Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LANCE BLADES & SCALPELS?

The FDA product code for LANCE BLADES & SCALPELS is GES.

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 Perry, Div. 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.

K851226I.V. START KITK844610PERRY SUTURING SET W/ANESTHETICK844609PERRY SUTURING SETK843125PERRY DERMAGUARD SURGICAL GLOVESK833920KELLY CHOLANGIOCATH

Related Devices (Code: GES)

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.

K032242PERSONNA PLUS SAFETY SCALPEL SYSTEMOmi Manufacturing Pty., Ltd.K932998EASY-ONDevon Industries, Inc.K923170LOS ALAMOS RETRACTABLE KNIFEInnovative Surgical Technology, Inc.K915119SCALPEL BLADE REMOVER (BLADEGARD)Intergrated Visual, Inc.K911913PRECISION GLIDE - ENHANCED SURGICAL BLADEBd Becton Dickinson Vacutainer Systems PreanalyticK900266STERILE CARBON STEEL SURGICAL BLADERahn Laboratories

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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