Universal Instru. Set for Neurovascular

FDA 510(k) K831071 · Prothia USA, Inc.

Substantially Equivalent

510(k) numberK831071

Submission

Device name
Universal Instru. Set for Neurovascular
Applicant
Prothia USA, Inc.
Mchenry, IL, US
Received
April 4, 1983
Decision date
June 8, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GZX – Instrument, Microsurgical
Device class
Class I (low risk)
Regulation
21 CFR 882.4525
Specialty
Neurology

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K932169Microsurgical InstrumentsGZX · Traditional American Russian Medical Services, Inc.07/20/1993SE
K926048Clarus Endoscopic Ball ProbeGZX · Traditional Clarus Medical Systems, Inc.04/07/1993SE
K911932J105 James Surgical System I/A PackGZX · Traditional O.R. Specialties, Inc.08/26/1991SE
K890216Microsurgical KeratomeGZX · Traditional Kinetic Medical Products02/16/1989SE
K873934Range of Crocodile Action InstrumentsGZX · Traditional Downs Surgical , Ltd.12/17/1987SE
K873933Range of Neurosurgical Instruments in TitaniumGZX · Traditional Downs Surgical , Ltd.12/17/1987SE
K862971Micra Microsurgical InstrumentsGZX · Traditional Cordis Corp.08/25/1986SE
K853179Vickers Ergomatic Microsur Instru-Univ R O L HandGZX · Traditional Keeler Instruments, Inc.11/07/1985SE
K853161The Vickers Standard Microsurgery SetGZX · Traditional Keeler Instruments, Inc.11/07/1985SE
K853181Vickers Ergomatic Micros Instr-Fine R or L HandedGZX · Traditional Keeler Instruments, Inc.10/28/1985SE

More from Keeler Instruments, Inc.

510(k)DeviceDecision
K830993AmpligreffeGFD · Traditional 05/03/1983SE
K823581Elpha 500GCJ · Traditional 03/24/1983SE
K830058Myograph 2000BXN · Traditional 03/07/1983SE
K823583Myotest Nerve StimulatorBXN · Traditional 12/30/1982SE

Questions and answers

When was Universal Instru. Set for Neurovascular cleared by the FDA?

Universal Instru. Set for Neurovascular (K831071) received a 510(k) decision of Substantially Equivalent on June 8, 1983, 65 days after the submission was received.

What is the product code of K831071?

The FDA product code is GZX – Instrument, Microsurgical, a Class I (low risk) device regulated under 21 CFR 882.4525.