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FDA 510(k)

NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280

K-Number: K860315 · 1986-06-17

ApplicantNeurotech, Inc.
Decision Date1986-06-17
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280 is the device name listed in this FDA 510(k) record. The listed applicant is Neurotech, Inc.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K860315. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280?

NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280 is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Neurotech, Inc.. The 510(k) number is K860315.

When did NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280 receive FDA 510(k) clearance?

NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280 received FDA 510(k) clearance on 1986-06-17, under 510(k) number K860315.

Who is the listed applicant for NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280?

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

What is the FDA product code for NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280?

The FDA product code for NEUROTECH-16 PROGRAM SYSTEM CONTROLLER MODEL 280 is IPF.

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Other records listing Neurotech, Inc. 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.

K955470ACTION POTENTIAL SIMULATION THERAPY DEVICEK860314NEUROTECH-4 PROGRAM NEUROMUSCULAR STIMULATOR 281

Related Devices (Code: IPF)

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.

K253542Apollo Quattro (APQ-10M)Weero Co., Ltd.K252816High Tone Power therapy (HiToP) (Model: HiToP PNP)Mohammadali NezakatiK260142StimelMD (SSMD) systemMotion Informatics ltd.K251083Compact IIEnraf-Nonius, B.V.K241433EVE Synergy (EVE-20M)Weero Co., Ltd.K241488TrainFES AdvanceTrainfes

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.

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