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FDA 510(k)

ACCUTECH ENDOLITE PROBE

K-Number: K061025 · 2006-05-31

ApplicantAccutech Medical Technologies, Inc.
Decision Date2006-05-31
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACCUTECH ENDOLITE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Accutech Medical Technologies, Inc.. It received FDA 510(k) clearance on 2006-05-31 under 510(k) number K061025. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTECH ENDOLITE PROBE?

ACCUTECH ENDOLITE PROBE is a medical device that received FDA 510(k) clearance on 2006-05-31. The listed applicant is Accutech Medical Technologies, Inc.. The 510(k) number is K061025.

When did ACCUTECH ENDOLITE PROBE receive FDA 510(k) clearance?

ACCUTECH ENDOLITE PROBE received FDA 510(k) clearance on 2006-05-31, under 510(k) number K061025.

Who is the listed applicant for ACCUTECH ENDOLITE PROBE?

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

What is the FDA product code for ACCUTECH ENDOLITE PROBE?

The FDA product code for ACCUTECH ENDOLITE PROBE is FFS.

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Other records listing Accutech Medical Technologies, Inc. as applicant

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Related Devices (Code: FFS)

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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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