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FDA 510(k)

DEFIANCE MODEL FUS 336

K-Number: K902685 · 1990-09-17

ApplicantDefiance Electronics, Inc.
Decision Date1990-09-17
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEFIANCE MODEL FUS 336 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 1990-09-17 under 510(k) number K902685. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEFIANCE MODEL FUS 336?

DEFIANCE MODEL FUS 336 is a medical device that received FDA 510(k) clearance on 1990-09-17. The listed applicant is Defiance Electronics, Inc.. The 510(k) number is K902685.

When did DEFIANCE MODEL FUS 336 receive FDA 510(k) clearance?

DEFIANCE MODEL FUS 336 received FDA 510(k) clearance on 1990-09-17, under 510(k) number K902685.

Who is the listed applicant for DEFIANCE MODEL FUS 336?

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 DEFIANCE MODEL FUS 336?

The FDA product code for DEFIANCE MODEL FUS 336 is EAZ.

Related Clinical Trials

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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.

K934815AIR COMPRESSOR, MODEL PAC 6.7

Related Devices (Code: EAZ)

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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