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FDA 510(k)

MAXI-MISER HUMIDIFIER INSERT 1020

K-Number: K841569 · 1984-05-30

ApplicantNova-Ventrx
Decision Date1984-05-30
Product Code
DecisionSubstantially Equivalent

Device Summary

MAXI-MISER HUMIDIFIER INSERT 1020 is the device name listed in this FDA 510(k) record. The listed applicant is Nova-Ventrx. It received FDA 510(k) clearance on 1984-05-30 under 510(k) number K841569. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXI-MISER HUMIDIFIER INSERT 1020?

MAXI-MISER HUMIDIFIER INSERT 1020 is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Nova-Ventrx. The 510(k) number is K841569.

When did MAXI-MISER HUMIDIFIER INSERT 1020 receive FDA 510(k) clearance?

MAXI-MISER HUMIDIFIER INSERT 1020 received FDA 510(k) clearance on 1984-05-30, under 510(k) number K841569.

Who is the listed applicant for MAXI-MISER HUMIDIFIER INSERT 1020?

The FDA 510(k) record lists Nova-Ventrx as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Nova-Ventrx 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.

K952267CRITERION, CRITERION I.V., MODIFIEDK954480CONDENSATE COLLECTION KITK893760CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004K881207RES-Q 1, 2, 3, 4 AND 5K870382DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011K863756MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT

View all 12 devices →

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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