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FDA 510(k)

ULTRACUT 2000

K-Number: K960374 · 1996-06-28

ApplicantUltralase Technologies, Inc.
Decision Date1996-06-28
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

ULTRACUT 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Ultralase Technologies, Inc.. It received FDA 510(k) clearance on 1996-06-28 under 510(k) number K960374. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRACUT 2000?

ULTRACUT 2000 is a medical device that received FDA 510(k) clearance on 1996-06-28. The listed applicant is Ultralase Technologies, Inc.. The 510(k) number is K960374.

When did ULTRACUT 2000 receive FDA 510(k) clearance?

ULTRACUT 2000 received FDA 510(k) clearance on 1996-06-28, under 510(k) number K960374.

Who is the listed applicant for ULTRACUT 2000?

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

What is the FDA product code for ULTRACUT 2000?

The FDA product code for ULTRACUT 2000 is LFL.

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Related Devices (Code: LFL)

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

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