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FDA 510(k)

SKYTRON ELITE SURGICAL TABLES

K-Number: K811311 · 1981-06-02

ApplicantSkytron, Div. the Kmw Group, Inc.
Decision Date1981-06-02
Product CodeGBC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKYTRON ELITE 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 1981-06-02 under 510(k) number K811311. The device is classified under product code GBC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKYTRON ELITE SURGICAL TABLES?

SKYTRON ELITE SURGICAL TABLES is a medical device that received FDA 510(k) clearance on 1981-06-02. The listed applicant is Skytron, Div. the Kmw Group, Inc.. The 510(k) number is K811311.

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

SKYTRON ELITE SURGICAL TABLES received FDA 510(k) clearance on 1981-06-02, under 510(k) number K811311.

Who is the listed applicant for SKYTRON ELITE 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 SURGICAL TABLES?

The FDA product code for SKYTRON ELITE SURGICAL TABLES is GBC.

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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: GBC)

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.

K896961HALUX EXLITE MINOR SURGERY LIGHTJedmed Instrument Co.K830610FLAT SUCTION DRAINSil-Med Corp.K810207MINOR SURGERY LIGHTCavitron 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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