FDA 510(k)

SECHRIST INFANT VENTRILATOR MODEL IV-100

K-Number: K811141 · 1981-06-12

Decision Date1981-06-12

Product CodeCBK

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SECHRIST INFANT VENTRILATOR MODEL IV-100 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 1981-06-12 under 510(k) number K811141. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECHRIST INFANT VENTRILATOR MODEL IV-100?

SECHRIST INFANT VENTRILATOR MODEL IV-100 is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K811141.

When did SECHRIST INFANT VENTRILATOR MODEL IV-100 receive FDA 510(k) clearance?

SECHRIST INFANT VENTRILATOR MODEL IV-100 received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811141.

Who is the listed applicant for SECHRIST INFANT VENTRILATOR MODEL IV-100?

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 SECHRIST INFANT VENTRILATOR MODEL IV-100?

The FDA product code for SECHRIST INFANT VENTRILATOR MODEL IV-100 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.