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FDA 510(k)

SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION

K-Number: K850563 · 1985-03-12

ApplicantNautilus Environmedical Systems, Inc.
Decision Date1985-03-12
Product CodeCBF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION is the device name listed in this FDA 510(k) record. The listed applicant is Nautilus Environmedical Systems, Inc.. It received FDA 510(k) clearance on 1985-03-12 under 510(k) number K850563. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION?

SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is Nautilus Environmedical Systems, Inc.. The 510(k) number is K850563.

When did SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION receive FDA 510(k) clearance?

SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION received FDA 510(k) clearance on 1985-03-12, under 510(k) number K850563.

Who is the listed applicant for SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION?

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

What is the FDA product code for SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION?

The FDA product code for SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION is CBF.

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.

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Other records listing Nautilus Environmedical Systems, 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.

K832127NAUTILUS MONOPLACE HYPERBARIC UNIT

Related Devices (Code: CBF)

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.

K240569FESL FINK Chamber; FEDL FINK Chamber; FETL FINK ChamberFink Engineering Pty, Ltd.K220290Revitalair 430+Us Hyperbaric NetworkK171899Revitalair 430FOxavita SrlK163109OxyHeal 4000 Multiplace Hyperbaric Chamber FamilyOxyheal Medical Systems, Inc.K152223Rectangular Multiplace Hyperbaric Chamber System Product Family with Touchscreen Control SystemOxyheal Medical Systems, Inc.K102831RSI 4200Reimers Systems, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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