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FDA 510(k)

THE INFANT FLOW SYSTEM

K-Number: K930713 · 1993-09-16

ApplicantSechrist Industries, Inc.
Decision Date1993-09-16
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE INFANT FLOW SYSTEM 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 1993-09-16 under 510(k) number K930713. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE INFANT FLOW SYSTEM?

THE INFANT FLOW SYSTEM is a medical device that received FDA 510(k) clearance on 1993-09-16. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K930713.

When did THE INFANT FLOW SYSTEM receive FDA 510(k) clearance?

THE INFANT FLOW SYSTEM received FDA 510(k) clearance on 1993-09-16, under 510(k) number K930713.

Who is the listed applicant for THE INFANT FLOW SYSTEM?

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 THE INFANT FLOW SYSTEM?

The FDA product code for THE INFANT FLOW SYSTEM is CAI.

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Other records listing Sechrist Industries, Inc. as applicant

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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.

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