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FDA 510(k)

VENTILATORY EFFORT MONITOR

K-Number: K810153 · 1981-02-09

ApplicantMedicon, Inc.
Decision Date1981-02-09
Product CodeFLS
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILATORY EFFORT MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Medicon, Inc.. It received FDA 510(k) clearance on 1981-02-09 under 510(k) number K810153. The device is classified under product code FLS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTILATORY EFFORT MONITOR?

VENTILATORY EFFORT MONITOR is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Medicon, Inc.. The 510(k) number is K810153.

When did VENTILATORY EFFORT MONITOR receive FDA 510(k) clearance?

VENTILATORY EFFORT MONITOR received FDA 510(k) clearance on 1981-02-09, under 510(k) number K810153.

Who is the listed applicant for VENTILATORY EFFORT MONITOR?

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

What is the FDA product code for VENTILATORY EFFORT MONITOR?

The FDA product code for VENTILATORY EFFORT MONITOR is FLS.

Related Clinical Trials

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.

Other records listing Medicon, 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.

View all 14 devices →

Related Devices (Code: FLS)

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.

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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