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FDA 510(k)

UNION BROACH BLEACHING LIGHT

K-Number: K895174 · 1990-04-13

ApplicantUnion Broach, Div. Moyco Industries, Inc.
Decision Date1990-04-13
Product CodeEEG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNION BROACH BLEACHING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. It received FDA 510(k) clearance on 1990-04-13 under 510(k) number K895174. The device is classified under product code EEG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNION BROACH BLEACHING LIGHT?

UNION BROACH BLEACHING LIGHT is a medical device that received FDA 510(k) clearance on 1990-04-13. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. The 510(k) number is K895174.

When did UNION BROACH BLEACHING LIGHT receive FDA 510(k) clearance?

UNION BROACH BLEACHING LIGHT received FDA 510(k) clearance on 1990-04-13, under 510(k) number K895174.

Who is the listed applicant for UNION BROACH BLEACHING LIGHT?

The FDA 510(k) record lists Union Broach, Div. Moyco Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNION BROACH BLEACHING LIGHT?

The FDA product code for UNION BROACH BLEACHING LIGHT is EEG.

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Other records listing Union Broach, Div. Moyco Industries, Inc. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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