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FDA 510(k)

ARMBOARD AND THE BOARD

K-Number: K833664 · 1983-12-27

ApplicantRick Robbin & Frederick Auerbach
Decision Date1983-12-27
Product CodeBTX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARMBOARD AND THE BOARD is the device name listed in this FDA 510(k) record. The listed applicant is Rick Robbin & Frederick Auerbach. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833664. The device is classified under product code BTX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARMBOARD AND THE BOARD?

ARMBOARD AND THE BOARD is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Rick Robbin & Frederick Auerbach. The 510(k) number is K833664.

When did ARMBOARD AND THE BOARD receive FDA 510(k) clearance?

ARMBOARD AND THE BOARD received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833664.

Who is the listed applicant for ARMBOARD AND THE BOARD?

The FDA 510(k) record lists Rick Robbin & Frederick Auerbach as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARMBOARD AND THE BOARD?

The FDA product code for ARMBOARD AND THE BOARD is BTX.

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Related Devices (Code: BTX)

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.

K935098BABY BOARDSentry Medical Products, Inc.K9001754/1 ARMBOARDInfection Control Products, Inc.K884838ALLEN PRONE ARMBOARDEdgewater Medical Systems, Inc.K882524UNIVERSALLY ADJUSTABLE ARMBOARDKarlin Technology, Inc.K881292ALLEN LATERAL ARMBOARDEdgewater Medical Systems, Inc.K864670BOARD, ARM (WITH COVER)Anago, 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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