FDA 510(k)

QUIK FLOW

K-Number: K921955 · 1993-01-29

ApplicantCalifornia Medical Equipment, Inc.

Decision Date1993-01-29

Product CodeFOZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

QUIK FLOW is the device name listed in this FDA 510(k) record. The listed applicant is California Medical Equipment, Inc.. It received FDA 510(k) clearance on 1993-01-29 under 510(k) number K921955. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIK FLOW?

QUIK FLOW is a medical device that received FDA 510(k) clearance on 1993-01-29. The listed applicant is California Medical Equipment, Inc.. The 510(k) number is K921955.

When did QUIK FLOW receive FDA 510(k) clearance?

QUIK FLOW received FDA 510(k) clearance on 1993-01-29, under 510(k) number K921955.

Who is the listed applicant for QUIK FLOW?

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

What is the FDA product code for QUIK FLOW?

The FDA product code for QUIK FLOW is FOZ.

Related Devices (Code: FOZ)

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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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.