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FDA 510(k)

MODEL LS-85 & MEDEL 1828 LINESCAN VISCO

K-Number: K822926 · 1982-11-24

ApplicantHoneywell, Inc.
Decision Date1982-11-24
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL LS-85 & MEDEL 1828 LINESCAN VISCO is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1982-11-24 under 510(k) number K822926. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL LS-85 & MEDEL 1828 LINESCAN VISCO?

MODEL LS-85 & MEDEL 1828 LINESCAN VISCO is a medical device that received FDA 510(k) clearance on 1982-11-24. The listed applicant is Honeywell, Inc.. The 510(k) number is K822926.

When did MODEL LS-85 & MEDEL 1828 LINESCAN VISCO receive FDA 510(k) clearance?

MODEL LS-85 & MEDEL 1828 LINESCAN VISCO received FDA 510(k) clearance on 1982-11-24, under 510(k) number K822926.

Who is the listed applicant for MODEL LS-85 & MEDEL 1828 LINESCAN VISCO?

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

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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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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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