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FDA 510(k)

MINI LED AUTOFOCUS

K-Number: K072181 · 2007-09-19

ApplicantSatelec
Decision Date2007-09-19
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINI LED AUTOFOCUS is the device name listed in this FDA 510(k) record. The listed applicant is Satelec. It received FDA 510(k) clearance on 2007-09-19 under 510(k) number K072181. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI LED AUTOFOCUS?

MINI LED AUTOFOCUS is a medical device that received FDA 510(k) clearance on 2007-09-19. The listed applicant is Satelec. The 510(k) number is K072181.

When did MINI LED AUTOFOCUS receive FDA 510(k) clearance?

MINI LED AUTOFOCUS received FDA 510(k) clearance on 2007-09-19, under 510(k) number K072181.

Who is the listed applicant for MINI LED AUTOFOCUS?

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

What is the FDA product code for MINI LED AUTOFOCUS?

The FDA product code for MINI LED AUTOFOCUS is EBZ.

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Other records listing Satelec as applicant

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Related Devices (Code: EBZ)

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

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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