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FDA 510(k)

SKYTRON ELITE 6000 & 6001 SURGICAL TABLES

K-Number: K853480 · 1985-09-12

ApplicantSkytron, Div. the Kmw Group, Inc.
Decision Date1985-09-12
Product CodeGDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKYTRON ELITE 6000 & 6001 SURGICAL TABLES 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 1985-09-12 under 510(k) number K853480. The device is classified under product code GDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKYTRON ELITE 6000 & 6001 SURGICAL TABLES?

SKYTRON ELITE 6000 & 6001 SURGICAL TABLES is a medical device that received FDA 510(k) clearance on 1985-09-12. The listed applicant is Skytron, Div. the Kmw Group, Inc.. The 510(k) number is K853480.

When did SKYTRON ELITE 6000 & 6001 SURGICAL TABLES receive FDA 510(k) clearance?

SKYTRON ELITE 6000 & 6001 SURGICAL TABLES received FDA 510(k) clearance on 1985-09-12, under 510(k) number K853480.

Who is the listed applicant for SKYTRON ELITE 6000 & 6001 SURGICAL TABLES?

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 ELITE 6000 & 6001 SURGICAL TABLES?

The FDA product code for SKYTRON ELITE 6000 & 6001 SURGICAL TABLES is GDC.

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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: GDC)

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.

K971390QUANTUM 3080SP SURGICAL TABLESTERIS CorporationK970807MOBILE OPERATING TABLE 1132.01Stierlen-Maquet AGK964273DURA-BOARD ARMBOARDAllen Medical Systems, Inc.K940616SKYTRON ELITE 3500 TABLESkytron, Div. the Kmw Group, Inc.K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.K914758MDT/SHAMPAINE MODEL 4900B SURGICAL TABLEMdt Corp., Inc.

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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