FDA 510(k)

MILLENNIUM INFANT VENTILATOR

K-Number: K993167 · 1999-11-10

Decision Date1999-11-10

Product CodeCBK

Advisory CommitteeAN

DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

MILLENNIUM INFANT VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sechrist Industries, Inc.. It received FDA 510(k) clearance on 1999-11-10 under 510(k) number K993167. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the MILLENNIUM INFANT VENTILATOR?

MILLENNIUM INFANT VENTILATOR is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K993167.

When did MILLENNIUM INFANT VENTILATOR receive FDA 510(k) clearance?

MILLENNIUM INFANT VENTILATOR received FDA 510(k) clearance on 1999-11-10, under 510(k) number K993167.

Who is the listed applicant for MILLENNIUM INFANT VENTILATOR?

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

What is the FDA product code for MILLENNIUM INFANT VENTILATOR?

The FDA product code for MILLENNIUM INFANT VENTILATOR is CBK.

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Other records listing Sechrist Industries, Inc. as applicant

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Related Devices (Code: CBK)

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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.