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FDA 510(k)

LOS ALAMOS RETRACTABLE KNIFE

K-Number: K923170 · 1993-02-18

ApplicantInnovative Surgical Technology, Inc.
Decision Date1993-02-18
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LOS ALAMOS RETRACTABLE KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Surgical Technology, Inc.. It received FDA 510(k) clearance on 1993-02-18 under 510(k) number K923170. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOS ALAMOS RETRACTABLE KNIFE?

LOS ALAMOS RETRACTABLE KNIFE is a medical device that received FDA 510(k) clearance on 1993-02-18. The listed applicant is Innovative Surgical Technology, Inc.. The 510(k) number is K923170.

When did LOS ALAMOS RETRACTABLE KNIFE receive FDA 510(k) clearance?

LOS ALAMOS RETRACTABLE KNIFE received FDA 510(k) clearance on 1993-02-18, under 510(k) number K923170.

Who is the listed applicant for LOS ALAMOS RETRACTABLE KNIFE?

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

What is the FDA product code for LOS ALAMOS RETRACTABLE KNIFE?

The FDA product code for LOS ALAMOS RETRACTABLE KNIFE is GES.

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Related Devices (Code: GES)

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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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