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FDA 510(k)

ARMBOARD

K-Number: K833559 · 1984-01-03

ApplicantMtd, Inc.
Decision Date1984-01-03
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARMBOARD is the device name listed in this FDA 510(k) record. The listed applicant is Mtd, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833559. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARMBOARD?

ARMBOARD is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Mtd, Inc.. The 510(k) number is K833559.

When did ARMBOARD receive FDA 510(k) clearance?

ARMBOARD received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833559.

Who is the listed applicant for ARMBOARD?

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

What is the FDA product code for ARMBOARD?

The FDA product code for ARMBOARD is KPR.

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Other records listing Mtd, 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.

K063439MEDICAL IMAGE MANAGEMENT DEVICES FOR VISION TOOLSK791374THE MTD VARA SET CASETTE HOLDERK772321ARTHROSTRESSK771659PATIENT RESTRAINT SYSTEM

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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