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FDA 510(k)

AIR COMPRESSOR, MODEL PAC 6.7

K-Number: K934815 · 1994-02-01

ApplicantDefiance Electronics, Inc.
Decision Date1994-02-01
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AIR COMPRESSOR, MODEL PAC 6.7 is the device name listed in this FDA 510(k) record. The listed applicant is Defiance Electronics, Inc.. It received FDA 510(k) clearance on 1994-02-01 under 510(k) number K934815. 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 AIR COMPRESSOR, MODEL PAC 6.7?

AIR COMPRESSOR, MODEL PAC 6.7 is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Defiance Electronics, Inc.. The 510(k) number is K934815.

When did AIR COMPRESSOR, MODEL PAC 6.7 receive FDA 510(k) clearance?

AIR COMPRESSOR, MODEL PAC 6.7 received FDA 510(k) clearance on 1994-02-01, under 510(k) number K934815.

Who is the listed applicant for AIR COMPRESSOR, MODEL PAC 6.7?

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

What is the FDA product code for AIR COMPRESSOR, MODEL PAC 6.7?

The FDA product code for AIR COMPRESSOR, MODEL PAC 6.7 is EIA.

Related Clinical Trials

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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Other records listing Defiance 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.

K902685DEFIANCE MODEL FUS 336

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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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