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FDA 510(k)

CANDELA MINIBRUSH

K-Number: K932930 · 1993-10-05

ApplicantCandela Laser Corp.
Decision Date1993-10-05
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CANDELA MINIBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Candela Laser Corp.. It received FDA 510(k) clearance on 1993-10-05 under 510(k) number K932930. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANDELA MINIBRUSH?

CANDELA MINIBRUSH is a medical device that received FDA 510(k) clearance on 1993-10-05. The listed applicant is Candela Laser Corp.. The 510(k) number is K932930.

When did CANDELA MINIBRUSH receive FDA 510(k) clearance?

CANDELA MINIBRUSH received FDA 510(k) clearance on 1993-10-05, under 510(k) number K932930.

Who is the listed applicant for CANDELA MINIBRUSH?

The FDA 510(k) record lists Candela Laser Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANDELA MINIBRUSH?

The FDA product code for CANDELA MINIBRUSH is FEB.

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Other records listing Candela Laser Corp. 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: FEB)

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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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