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FDA 510(k)

RES Q AIR SYSTEM MODEL HT-1000

K-Number: K926161 · 1993-08-26

ApplicantC.F. Electronics, Inc.
Decision Date1993-08-26
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RES Q AIR SYSTEM MODEL HT-1000 is the device name listed in this FDA 510(k) record. The listed applicant is C.F. Electronics, Inc.. It received FDA 510(k) clearance on 1993-08-26 under 510(k) number K926161. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RES Q AIR SYSTEM MODEL HT-1000?

RES Q AIR SYSTEM MODEL HT-1000 is a medical device that received FDA 510(k) clearance on 1993-08-26. The listed applicant is C.F. Electronics, Inc.. The 510(k) number is K926161.

When did RES Q AIR SYSTEM MODEL HT-1000 receive FDA 510(k) clearance?

RES Q AIR SYSTEM MODEL HT-1000 received FDA 510(k) clearance on 1993-08-26, under 510(k) number K926161.

Who is the listed applicant for RES Q AIR SYSTEM MODEL HT-1000?

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

What is the FDA product code for RES Q AIR SYSTEM MODEL HT-1000?

The FDA product code for RES Q AIR SYSTEM MODEL HT-1000 is BTT.

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Other records listing C.F. Electronics, Inc. as applicant

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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Related Devices (Code: BTT)

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.

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