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FDA 510(k)

KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR

K-Number: K851627 · 1985-11-08

ApplicantEaton Medical Group
Decision Date1985-11-08
Product CodeDRW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR is the device name listed in this FDA 510(k) record. The listed applicant is Eaton Medical Group. It received FDA 510(k) clearance on 1985-11-08 under 510(k) number K851627. The device is classified under product code DRW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR?

KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR is a medical device that received FDA 510(k) clearance on 1985-11-08. The listed applicant is Eaton Medical Group. The 510(k) number is K851627.

When did KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR receive FDA 510(k) clearance?

KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR received FDA 510(k) clearance on 1985-11-08, under 510(k) number K851627.

Who is the listed applicant for KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR?

The FDA 510(k) record lists Eaton Medical Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR?

The FDA product code for KBX-20 OUTBOARD KEYBOARD ACCESS. FOR G-2000 ELECTR is DRW.

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Other records listing Eaton Medical Group 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.

K851623MODEL TRC-40 TELEMETRY RECIEVER MODULEK851624MODEL TT-185 TELEMETRY TRANSMITTERK851625SCX-10 SINGLE CHANNEL RECORDER ACCESS. FOR G-2000K851632PCX-100 PATIENT INPUT LEADWIREK851631TMX-C1/C2 TRADMILL CONTROLLER ACCESS.K851630TMX-80 TREADMILL

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Related Devices (Code: DRW)

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.

K033513EASI ECG ALGORITHMPhilips Medical SystemsK020456EASI 12 LEAD ALGORITHMPhilips Medical SystemsK930786EPCORSiemens Medical Solutions USA, Inc.K872781EASI LEAD SYSTEM CABLE ASSEMBLYTotemite Medical ElectronicsK861981ELECTROCARDIOGRAPH LEAD SWITCHING ADAPTORVital Signs, Inc.K851632PCX-100 PATIENT INPUT LEADWIREEaton Medical Group

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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