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FDA 510(k)

1,2,3 CHANNELL RECORDERS (AR150,AR250,-)

K-Number: K810166 · 1981-02-25

ApplicantHoneywell, Inc.
Decision Date1981-02-25
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

1,2,3 CHANNELL RECORDERS (AR150,AR250,-) is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-02-25 under 510(k) number K810166. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1,2,3 CHANNELL RECORDERS (AR150,AR250,-)?

1,2,3 CHANNELL RECORDERS (AR150,AR250,-) is a medical device that received FDA 510(k) clearance on 1981-02-25. The listed applicant is Honeywell, Inc.. The 510(k) number is K810166.

When did 1,2,3 CHANNELL RECORDERS (AR150,AR250,-) receive FDA 510(k) clearance?

1,2,3 CHANNELL RECORDERS (AR150,AR250,-) received FDA 510(k) clearance on 1981-02-25, under 510(k) number K810166.

Who is the listed applicant for 1,2,3 CHANNELL RECORDERS (AR150,AR250,-)?

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

What is the FDA product code for 1,2,3 CHANNELL RECORDERS (AR150,AR250,-)?

The FDA product code for 1,2,3 CHANNELL RECORDERS (AR150,AR250,-) is DSF.

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Other records listing Honeywell, 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.

K902230COLORADO COLOR IMAGING RECORDERK863100CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECORK853501HONEYWELL ELECTRONIC VENTILATOR EV-AK855125PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEMK851888APM DISPOS. BLOOD PRESSURE TRANSDUCERK851496ECG MONITOR MODEL RM102

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Related Devices (Code: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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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