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FDA 510(k)

SURGACTIVATOR

K-Number: K951569 · 1995-06-06

ApplicantDeschutes Medical Products, Inc.
Decision Date1995-06-06
Product CodeLJH
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGACTIVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Deschutes Medical Products, Inc.. It received FDA 510(k) clearance on 1995-06-06 under 510(k) number K951569. The device is classified under product code LJH. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGACTIVATOR?

SURGACTIVATOR is a medical device that received FDA 510(k) clearance on 1995-06-06. The listed applicant is Deschutes Medical Products, Inc.. The 510(k) number is K951569.

When did SURGACTIVATOR receive FDA 510(k) clearance?

SURGACTIVATOR received FDA 510(k) clearance on 1995-06-06, under 510(k) number K951569.

Who is the listed applicant for SURGACTIVATOR?

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

What is the FDA product code for SURGACTIVATOR?

The FDA product code for SURGACTIVATOR is LJH.

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Other records listing Deschutes Medical Products, Inc. as applicant

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Related Devices (Code: LJH)

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K254111Irrigation/Urology SetsB.Braun Medical, Inc.K162992Karl Storz UROMAT E.A.S.I.Karl Storz Endoscopy America, Inc.K070873AMSURE BLADDER IRRIGATION SETAmsino Intl., Inc.K071832MODIFCATION TO: SPYGLASS IRRIGATION SYSTEMMedical Scientific, Inc.K063700SPYGLASS IRRIGATION SYSTEMMedical Scientific, Inc.K062551NEXUS IRRIGATION TUBING SETNexus Medical, LLC

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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