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FDA 510(k)

SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI

K-Number: K900472 · 1990-09-04

ApplicantSkytron, Div. the Kmw Group, Inc.
Decision Date1990-09-04
Product CodeHBN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI is the device name listed in this FDA 510(k) record. The listed applicant is Skytron, Div. the Kmw Group, Inc.. It received FDA 510(k) clearance on 1990-09-04 under 510(k) number K900472. The device is classified under product code HBN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI?

SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI is a medical device that received FDA 510(k) clearance on 1990-09-04. The listed applicant is Skytron, Div. the Kmw Group, Inc.. The 510(k) number is K900472.

When did SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI receive FDA 510(k) clearance?

SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI received FDA 510(k) clearance on 1990-09-04, under 510(k) number K900472.

Who is the listed applicant for SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI?

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

What is the FDA product code for SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI?

The FDA product code for SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI is HBN.

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Other records listing Skytron, Div. the Kmw Group, 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.

K071698AURORA LED SERIES SURGICAL LIGHTSK021585STELLAR SERIES SURGICAL LIGHTS WITH HERMESK002463STELLARK992090MILLENNIUM GOLDK950192SKYTRON SKYBOOM SERIESK940616SKYTRON ELITE 3500 TABLE

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Related Devices (Code: HBN)

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.

K822426MCINTYRE MICROSCOPE STANDSurgi-Quip Inc.UK822428SURGI-QUIP MICROSCOPE STANDSurgi-Quip Inc.UK822012BINOCULAR OPERATING MICROSCOPES &Kelleher Corp.

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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