Universal Instru. Set for Neurovascular
FDA 510(k) K831071 · Prothia USA, Inc.
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)
Other 510(k)s with product code GZX
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|---|---|---|---|
| K932169 | Microsurgical InstrumentsGZX · Traditional | American Russian Medical Services, Inc. | 07/20/1993SE |
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| K911932 | J105 James Surgical System I/A PackGZX · Traditional | O.R. Specialties, Inc. | 08/26/1991SE |
| K890216 | Microsurgical KeratomeGZX · Traditional | Kinetic Medical Products | 02/16/1989SE |
| K873934 | Range of Crocodile Action InstrumentsGZX · Traditional | Downs Surgical , Ltd. | 12/17/1987SE |
| K873933 | Range of Neurosurgical Instruments in TitaniumGZX · Traditional | Downs Surgical , Ltd. | 12/17/1987SE |
| K862971 | Micra Microsurgical InstrumentsGZX · Traditional | Cordis Corp. | 08/25/1986SE |
| K853179 | Vickers Ergomatic Microsur Instru-Univ R O L HandGZX · Traditional | Keeler Instruments, Inc. | 11/07/1985SE |
| K853161 | The Vickers Standard Microsurgery SetGZX · Traditional | Keeler Instruments, Inc. | 11/07/1985SE |
| K853181 | Vickers Ergomatic Micros Instr-Fine R or L HandedGZX · Traditional | Keeler Instruments, Inc. | 10/28/1985SE |
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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.