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FDA 510(k)

FLOW=MED

K-Number: K924322 · 1994-04-26

Decision Date1994-04-26
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOW=MED is the device name listed in this FDA 510(k) record. The listed applicant is International Electronic Technology Corp.. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K924322. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW=MED?

FLOW=MED is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is International Electronic Technology Corp.. The 510(k) number is K924322.

When did FLOW=MED receive FDA 510(k) clearance?

FLOW=MED received FDA 510(k) clearance on 1994-04-26, under 510(k) number K924322.

Who is the listed applicant for FLOW=MED?

The FDA 510(k) record lists International Electronic Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOW=MED?

The FDA product code for FLOW=MED is BZH.

Related Devices (Code: BZH)

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.

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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