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FDA 510(k)

MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE

K-Number: K911901 · 1991-07-26

ApplicantStortz
Decision Date1991-07-26
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Stortz. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K911901. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE?

MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Stortz. The 510(k) number is K911901.

When did MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE receive FDA 510(k) clearance?

MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE received FDA 510(k) clearance on 1991-07-26, under 510(k) number K911901.

Who is the listed applicant for MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE?

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

What is the FDA product code for MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE?

The FDA product code for MAXI CABINET OPTIONAL BUILT IN S6000 LIGHT SOURCE is ETF.

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Related Devices (Code: ETF)

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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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