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FDA 510(k)

MEDDARS/ULTRA IMAGER PULSE/PHON MODULE

K-Number: K811626 · 1981-07-01

ApplicantHoneywell, Inc.
Decision Date1981-07-01
Product CodeDQC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDDARS/ULTRA IMAGER PULSE/PHON MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-07-01 under 510(k) number K811626. The device is classified under product code DQC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDDARS/ULTRA IMAGER PULSE/PHON MODULE?

MEDDARS/ULTRA IMAGER PULSE/PHON MODULE is a medical device that received FDA 510(k) clearance on 1981-07-01. The listed applicant is Honeywell, Inc.. The 510(k) number is K811626.

When did MEDDARS/ULTRA IMAGER PULSE/PHON MODULE receive FDA 510(k) clearance?

MEDDARS/ULTRA IMAGER PULSE/PHON MODULE received FDA 510(k) clearance on 1981-07-01, under 510(k) number K811626.

Who is the listed applicant for MEDDARS/ULTRA IMAGER PULSE/PHON MODULE?

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 MEDDARS/ULTRA IMAGER PULSE/PHON MODULE?

The FDA product code for MEDDARS/ULTRA IMAGER PULSE/PHON MODULE is DQC.

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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: DQC)

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.

K950537CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPHCardiophonics, Inc.K952651LIFE SOUND SENSORFlowscan, Inc.K943726ACOUSTIC RECORDERTechnology Applications Assoc., Inc.K924054PHONOCARDIOGRAPHEcho UltrasoundK902185DYNAMIC SPECTRAL PHONOCARDIOGRAPHReeves Scientific, Inc.K900560ACUSON HEARTSOUND/PULSE/RESPIRATION MODULEAcuson Corp.

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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