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FDA 510(k)

MAHLER ABDOMINAL WALL ELEVATOR

K-Number: K960878 · 1996-03-15

ApplicantCook Urological, Inc.
Decision Date1996-03-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAHLER ABDOMINAL WALL ELEVATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1996-03-15 under 510(k) number K960878. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAHLER ABDOMINAL WALL ELEVATOR?

MAHLER ABDOMINAL WALL ELEVATOR is a medical device that received FDA 510(k) clearance on 1996-03-15. The listed applicant is Cook Urological, Inc.. The 510(k) number is K960878.

When did MAHLER ABDOMINAL WALL ELEVATOR receive FDA 510(k) clearance?

MAHLER ABDOMINAL WALL ELEVATOR received FDA 510(k) clearance on 1996-03-15, under 510(k) number K960878.

Who is the listed applicant for MAHLER ABDOMINAL WALL ELEVATOR?

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

What is the FDA product code for MAHLER ABDOMINAL WALL ELEVATOR?

The FDA product code for MAHLER ABDOMINAL WALL ELEVATOR is GCJ.

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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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