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FDA 510(k)

MODEL SIX BEAM SYSTEM

K-Number: K811848 · 1981-09-08

ApplicantBraintech, Inc.
Decision Date1981-09-08
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL SIX BEAM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Braintech, Inc.. It received FDA 510(k) clearance on 1981-09-08 under 510(k) number K811848. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL SIX BEAM SYSTEM?

MODEL SIX BEAM SYSTEM is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Braintech, Inc.. The 510(k) number is K811848.

When did MODEL SIX BEAM SYSTEM receive FDA 510(k) clearance?

MODEL SIX BEAM SYSTEM received FDA 510(k) clearance on 1981-09-08, under 510(k) number K811848.

Who is the listed applicant for MODEL SIX BEAM SYSTEM?

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

What is the FDA product code for MODEL SIX BEAM SYSTEM?

The FDA product code for MODEL SIX BEAM SYSTEM is GWF.

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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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