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FDA 510(k)

DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT

K-Number: K940599 · 1994-04-29

ApplicantQ. C. Filter, Inc.
Decision Date1994-04-29
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Q. C. Filter, Inc.. It received FDA 510(k) clearance on 1994-04-29 under 510(k) number K940599. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT?

DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT is a medical device that received FDA 510(k) clearance on 1994-04-29. The listed applicant is Q. C. Filter, Inc.. The 510(k) number is K940599.

When did DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT receive FDA 510(k) clearance?

DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT received FDA 510(k) clearance on 1994-04-29, under 510(k) number K940599.

Who is the listed applicant for DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT?

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

What is the FDA product code for DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT?

The FDA product code for DUAL AIR/WATER FILTER CARTRIDGE HANDLE KIT is EIA.

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Related Devices (Code: EIA)

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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.

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